Editors

Zvi Rappoport Zvi Rappoport is Professor Emeritus at the Institute of Chemistry at The Hebrew University of Jerusalem. He worked for great many years with the founding editor, Professor Saul Patai on The Chemistry of Functional Groups, eight of which he edited with Professor Patai. He has been the lead editor of the series since the death of Professor Patai editing around 50 volumes in the series. Joel F. Liebman Joel Liebman is Professor of Chemistry at the University of Maryland Baltimore County. A graduate of Princeton, he had held posts at Yale University, University of Utah and the University of South Carolina in the field of organic chemistry. He has been an editor on several volumes of the Patai series and contributed chapters to over 25 volumes. Ilan Marek Professor Ilan Marek is a graduate of University of Pierre-et-Marie Curie, Paris. He previously was the head of a research group at CNRS for 7 years. His specialist areas are organometallic chemistry applied to organic synthesis and steroselective synthesis. He currently has the Sir Michael and Lady Sobell Academic chair at the Schulich Faculty of Chemistry at Technion–Israel Institute of Technology. Contributors

Cyclopropyl Group (1995) John E. Baldwin Syracuse University, Department of Chemistry, Syracuse, NY 13244, USA Thermal Stereomutations of Cyclopropanes and Vinylcyclopropanes Ronald F. Childs McMaster University, Department of Chemistry, Hamilton, Ontario, Canada L8S 4M1 Cyclopropyl Homoconjugation—Experimental Facts and Interpretations Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspects and Analysis James Bryant Conant Harvard University, Department of Chemistry, Cambridge, MA, USA Prologue: History of Cyclopropane Derivatives Before 1916

Dieter Cremer University of Göteborg, Department of Theoretical Chemistry, Kemigården 3, Göteborg, Sweden S-41296 Cyclopropyl Homoconjugation—Experimental Facts and Interpretations Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspects and Analysis General and Theoretical Aspects of the Cyclopropyl Group George Elia McMaster University, Department of Chemistry, Hamilton, Ontario, Canada L8S 4M1 Cyclopropyl Homoconjugation—Experimental Facts and Interpretations Zeev Goldschmidt Bar–Ilan University, Department of Chemistry, Ramat–Gan 52900, Israel Organometallic Derivatives Brian Halton Victoria University of Wellington, Department of Chemistry, PO Box 600, Wellington, New Zealand Cycloproparenes Piotr Kaszynski Vanderbilt University, Department of Chemistry, Nashville, TN 37235, USA [1.1.1]Propellanes Elfi Kraka University of Göteborg, Department of Theoretical Chemistry, Kemigården 3, Göteborg, Sweden S-41296 Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspects and Analysis General and Theoretical Aspects of the Cyclopropyl Group Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 Wilkens Avenue, Baltimore, MA 21228–5398, USA Thermochemistry

Kirill A Lukin The University of Chicago, Department of Chemistry, 5735 South Ellis Avenue, Chicago, IL 60637, USA Spiroannulated Cyclopropanes M. Anthony McKervey The Queen's University, School of Chemistry, Belfast, Northern Ireland, UK BT9 5AG Metal Catalysed Cyclopropanation Josef Michl University of Colorado, Department of Chemistry and Biochemistry, Boulder, CO 80309-0215, USA [1.1.1]Propellanes Shinya Nishida Hokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan Recent Advances in Synthesis of Cyclopropanes Masakazu Ohkita Hokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan Recent Advances in Synthesis of Cyclopropanes George A. Olah University of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry, Los Angeles, CA 90089-1661, USA Long-Lived Cyclopropylcarbinyl Cations Prakash V. Reddy University of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry, Los Angeles, CA 90089-1661, USA Long-Lived Cyclopropylcarbinyl Cations Béla Rozsondai Research Group of the Hungarian Academy of Sciences, Eötvös University, P.O. Box 117, Budapest, Hungary H-1431 Structural Chemistry

G. K. Surya Prakash University of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry, Los Angeles, CA 90089-1661, USA Long-Lived Cyclopropylcarbinyl Cations Kalman Josef Szabo University of Göteborg, Department of Theoretical Chemistry, Kemigården 3, Göteborg, Sweden S-41296 General and Theoretical Aspects of the Cyclopropyl Group Takashi Tsuji Hokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan Recent Advances in Synthesis of Cyclopropanes Tao Ye The Queen's University, School of Chemistry, Belfast, Northern Ireland, UK BT9 5AG Metal Catalysed Cyclopropanation Nikolai S Zefirov Moscow State University, Department of Chemistry, Moscow, Russia Spiroannulated Cyclopropanes Howard E. Zimmerman University of Wisconsin, Chemistry Department, Madison, WI 53706, USA Cyclopropane Photochemistry

Halides, Pseudo-Halides and Azides (1995) Zeev B. Alfassi Ben Gurion University of the Negev, Department of Nuclear Engineering, Beer Sheva, Israel Radiation Chemistry Mark S. Baird University of Wales, Department of Chemistry, Gwynedd, Bangor, Wales, UK LL57 2UW

Eliminations Involving Carbon–Halogen Bonds and Leading to Highly Strained Rings Klara Berei KFKI Atomic Energy Research Institute, Budapest, Hungary Recent Advances in the Organic Chemistry of Astatine Ivan G. Bolesov Moscow State University, Department of Chemistry, Moscow, Russia Eliminations Involving Carbon–Halogen Bonds and Leading to Highly Strained Rings James H. Brewster Purdue University, Department of Chemistry, West Lafayette, IN 47907-3699, USA Conformational and Chiroptical Properties of Alkyl Halides Joseph Casanova California State University, Department of Chemistry, Los Angeles, CA 90032, USA Electrochemistry of the Carbon–Halogen Bond Gabriel Chuchani Instituto Venezolano de Investigaciones Científicas (IVIC), Department of Chemistry, Apartado 21827, Caracas, Venezuela 1020-A Pyrolysis of Organic Halides Jan Cornelisse Leiden Institute of Chemistry, Leiden University, Gorlaeus Laboratories, 2300 RA Leiden, The Netherlands 9502 Recent Advances in the Photochemistry of the Carbon–Halogen Bond Brian Everatt Ciba Geigy PLC, Hulley Road, Macclesfield, Cheshire, UK SK10 2NX NMR Spectroscopy Joseph S. Francisco Purdue University, Department of Chemistry and Department of Earth and Atmospheric Sciences, West Lafayette, IN, USA Atmospheric Chemistry of Organic Halides

Michel Geoffroy Université de Genève, Sciences II, Départment de Chimie Physique, 30 Quai Ernest-Ansermet, Genève 4, Switzerland 1211 Electron Spin Resonance and Nuclear Quadrupole Resonance James R. Green Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario, Canada N9B 3P4 Reactions of Organic Halides Mediated by Transition Metal Compounds Jeff Hoyle Nova Scotia Agricultural College, Chemistry and Soil Science Department, Truro, Nova Scotia, Canada B2 N 5E3 Some Synthetic Uses of Halides Marianna Kańska Warsaw University, Department of Chemistry, Warsaw, Poland Syntheses and Uses of Isotopically Labelled Organic Halides Kenneth L. Kirk National Institutes of Health, Department of Health & Human Services, Bethesda, MA 20892, USA Biochemistry of halogenated organic compounds L. Klasinc Institute Rugjer Bošković, Zagreb, Croatia Photoelectron Spectra of Compounds with Carbon–Halogen Bonds Gerald F. Koser The University of Akron, Department of Chemistry, Akron, OH 44325–3601, USA Halonium Ions Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 Wilkens Ave., Baltimore, MA 21228-5398, USA Thermochemistry

Gerrit Lodder Leiden Institute of Chemistry, Leiden University, Gorlaeus Laboratories, 2300 RA Leiden, The Netherlands 9502 Recent Advances in the Photochemistry of the Carbon–Halogen Bond Edwin A. C. Lucken Université de Genève, Sciences II, Départment de Chimie Physique, 30 Quai Ernest-Ansermet, Genève 4, Switzerland 1211 Electron Spin Resonance and Nuclear Quadrupole Resonance Hisham G. Lutfi southern Illinois University, Department of Chemistry and Biochemistry, Carbondale, IL 62901–4409, USA Positive Halogen Compounds W. Gary Mallard National Institute of Standards and Technology, Chemical Kinetics and Thermodynamics Division, Gaithersburg, MA 20899-0001, USA Thermochemistry S. P. McGlynn Louisiana State University, Department of Chemistry, Baton Rouge, LA 70803, USA Photoelectron Spectra of Compounds with Carbon–Halogen Bonds CAL Y. Meyers southern Illinois University, Department of Chemistry and Biochemistry, Carbondale, IL 62901–4409, USA Positive Halogen Compounds Jane S. Murray University of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA General and Theoretical Aspects of the C–X bonds (X = F, Cl, Br, I): Integration of Theory and Experiment I. Novak National University of Singapore, Department of Chemistry, Singapore Photoelectron Spectra of Compounds with Carbon–Halogen Bonds

Heinz Oberhammer Universität Tübingen, Institut für Physikalische und Theoretische Chemie, Tübingen, Germany 76072 Structural Chemistry Cristina Paradisi Centro Studio Meccanismi Reazioni Organiche del CNR, Dipartimento di Chimica Organica dell'Università, Via Marzolo 1, Padova, Italy 35131 Mass spectra and gas-phase ion chemistry of halogen-containing compounds R. V. Parish UMIST, Department of Chemistry, PO Box 88, Manchester, UK M60 1QD Mössbauer Spectroscopy Alicia B. Peñéñory Facultad de Ciencias Químicas, Departmento de Química Orgánica, Universidad Nacional de Córdoba, INFIQC, Suc. 16, CC 61, Córdoba, Argentina 5016 Recent Advances in the SRN1 Reaction of Organic Halides Adriana B. Pierini Facultad de Ciencias Químicas, Departmento de Química Orgánica, Universidad Nacional de Córdoba, INFIQC, Suc. 16, CC 61, Córdoba, Argentina 5016 Recent Advances in the SRN1 Reaction of Organic Halides Peter Politzer University of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA General and Theoretical Aspects of the C–X bonds (X = F, Cl, Br, I): Integration of Theory and Experiment V. Prakash Reddy University of Miami, Department of Chemistry, Coral Gables, FL 33124, USA Electrochemistry of the Carbon–Halogen Bond Roberto A. Rossi Facultad de Ciencias Químicas, Departmento de Química Orgánica, Universidad Nacional de Córdoba, INFIQC, Suc. 16, CC 61, Córdoba, Argentina 5016

Recent Advances in the SRN1 Reaction of Organic Halides Shlomo Rozen Tel Aviv University, School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv, Israel 69978 The Formation of the C–F Bond: The Last Twelve Years Yoel Sasson The Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Jerusalem, Israel 91904 Formation of Carbon–Halogen Bonds (Cl, Br, I) Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry Peter Taylor The Open University, Chemistry Department, Milton Keynes, Bucks, UK MK7 6AA NMR Spectroscopy László Vasáros KFKI Atomic Energy Research Institute, Budapest, Hungary Recent Advances in the Organic Chemistry of Astatine Umberto Vettori Centro Studio Stabilità e Reattività dei Composti di Coordinazione del CNR, Via Marzolo 1, Padova, Italy 35131 Mass spectra and gas-phase ion chemistry of halogen-containing compounds Ian H. Williams University of Bath, School of Chemistry, Bath, UK BA2 7AY Atmospheric Chemistry of Organic Halides Mieczysłlaw Zieliński Jagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland

Syntheses and Uses of Isotopically Labelled Organic Halides Marko Zupan University of Ljubljana, Laboratory for Organic and Bioorganic Chemistry, Department of Chemistry and `J. Stefan' Institute, Ljubljana, Slovenia Functionalization of Organic Molecules by Xenon Fluorides

Organic Germanium, Tin and Lead Compounds (1995) Harold Basch Bar-Ilan University, Department of Chemistry, Ramat-Gan 52900, Israel The Nature of the C–M Bond (M = Ge, Sn, Pb) Carla Cauletti Università di Roma `La Sapienza', Dipartimento di Chimica, Piazzale Aldo Moro, 5, Rome, Italy 00185 Photoelectron Spectroscopy (PES) of Organometallic Compounds with C–M (M=Ge, Sn, Pb) Bonds Marvin Charton School of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA Substituent Effects of Germanium, Tin and Lead Groups P. J. Craig De Montfort University, Department of Chemistry, The Gateway, Leicester, UK LE1 9BH The Environmental Methylation of Germanium, Tin and Lead Marcel Gielen Free University of Brussels, Pleinlaan 2, Brussels, Belgium B-1050 Synthesis of M(IV) Organometallic Compounds, where M = Ge, Sn, Pb Charles M. Gordon Dublin City University, School of Chemical Sciences, Dublin 9, Ireland The Photochemistry of Organometallic Compounds of Germanium and Lead Sarina Grinberg Institutes for Applied Research, Ben-Gurion University of the Negev, Beer-Sheva, Israel 84110 Analytical Aspects of Organogermanium Compounds Analytical Aspects of Organolead Compounds Analytical Aspects of Organotin Compounds

Tova Hoz Bar-Ilan University, Department of Chemistry, Ramat-Gan 52900, Israel The Nature of the C–M Bond (M = Ge, Sn, Pb) L. M. Ignatovich Latvian Institute of Organic Synthesis, Riga, Latvia LV 1006 Toxicity of Organogermanium Compounds Jim Iley The Open University, Physical Organic Chemistry Research Group, Chemistry Department, Milton Keynes, UK MK7 6AA ESR of Organogermanium, Organotin and Organolead Radicals Jill A. Jablonowski University of South Carolina, Department of Chemistry and Biochemistry, Columbia, SC 29208, USA Stereochemistry and Conformation of Organogermanium, Organotin and Organolead Compounds Helen Joly Laurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6 Syntheses and Uses of Isotopically Labelled Organic Derivatives of Ge, Sn and Pb Thomas M. Klapötke Technische Universität Berlin, Institut für Anorganische und Analytische Chemie, Strasse des 17. Juni 135, Berlin, Germany D-10623 Acidity, Complexing, Basicity and H-Bonding of Organic Germanium, Tin and Lead Compounds: Experimental and Computational Results Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland Baltimore County, 5401 Wilkens Avenue, Baltimore, MD 21228-5398, USA Thermochemistry Conor Long Dublin City University, School of Chemical Sciences, Dublin 9, Ireland

The Photochemistry of Organometallic Compounds of Germanium and Lead E. Lukevics Latvian Institute of Organic Synthesis, Riga, Latvia LV 1006 Toxicity of Organogermanium Compounds Kenneth M. Mackay University of Waikato, School of Science and Technology, Hamilton, New Zealand 3105 Structural Aspects of Compounds Containing C–E (E=Ge, Sn, Pb) Bonds Shigeru Maeda Faculty of Engineering, Kagoshima University, Department of Applied Chemistry and Chemical Engineering, 1-21-40 Korimoto, Kagoshima, Japan 890 Safety and Environmental Effects James A. Marshall University of South Carolina, Department of Chemistry and Biochemistry, Columbia, SC 29208, USA Stereochemistry and Conformation of Organogermanium, Organotin and Organolead Compounds José A. Martinho Simões Departmento de Química, Faculdade de Ciências, Universidade de Lisboa, 1700 Lisboa, Portugal Thermochemistry Michael Michman The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 The Electrochemistry of Alkyl Compounds of Germanium, Tin and Lead Axel Schulz Technische Universität Berlin, Institut für Anorganische und Analytische Chemie, Strasse des 17. Juni 135, Berlin, Germany D-10623 Acidity, Complexing, Basicity and H-Bonding of Organic Germanium, Tin and Lead Compounds: Experimental and Computational Results Larry R. Sherman University of Scranton, Department of Chemistry, Scranton, PA 18510 4626, USA Organotin Toxicology

Suzanne W. Slayden Department of Chemistry, George Mason University, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry Stefano Stranges Università di Roma `La Sapienza', Dipartimento di Chimica, Piazzale Aldo Moro, 5, Rome, Italy 00185 Photoelectron Spectroscopy (PES) of Organometallic Compounds with C–M (M=Ge, Sn, Pb) Bonds John M. Tsangaris University of Ioannina, Department of Chemistry, Ioannina, Greece GR-45100 Synthesis of M(IV) Organometallic Compounds, where M = Ge, Sn, Pb J. T. Van Elteren De Montfort University, Department of Chemistry, The Gateway, Leicester, UK LE1 9BH The Environmental Methylation of Germanium, Tin and Lead Kenneth C Westaway Laurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6 Syntheses and Uses of Isotopically Labelled Organic Derivatives of Ge, Sn and Pb Rudolph Willem Free University of Brussels, Pleinlaan 2, Brussels, Belgium B-1050 Synthesis of M(IV) Organometallic Compounds, where M = Ge, Sn, Pb Jacob Zabicky Institutes for Applied Research, Ben-Gurion University of the Negev, Beer-Sheva, Israel 84110 Analytical Aspects of Organogermanium Compounds Analytical Aspects of Organolead Compounds Analytical Aspects of Organotin Compounds

Amino, Nitroso, Nitro and Related Groups (1996)

Pinchas Aped Bar-Ilan University, Department of Chemistry, Israel 52900; Ramat-Gan Molecular Mechanics Calculations Shmuel Bittner Ben-Gurion University of the Negev, Institutes for Applied Research, Department of Chemistry, Beer-Sheva, Israel Analytical Aspects of Amino, Quaternary Ammonium, Nitro, Nitroso and Related Functional Groups Richard D. Bowen University of Bradford, Chemistry and Chemical Technology, Bradford, West Yorkshire, England, UK BD7 1DP The Chemistry of Ionized, Protonated and Cationated Amines in the Gas Phase G. V. Boyd The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 Advances in the Chemistry of Amino and Nitro Compounds Silvia Bradamante Università di Milano, CNR, Centro di studio sulla Sintesi e Stereochimica di Speciali Sistemi Organici, c/o Dipartimento di Chimica Organica e Industriale, via Golgi 19, Milano, Italia 20133 Acidity and Basicity Mary Stinecipher Campbell Los Alamos National Laboratory, DX-2 Explosive Science Technology, MS C920, Los Alamos, NM 87545-0000, USA Thermochemistry Lars Carlsen Department of Environmental Chemistry, National Environmental Research Institute, Roskilde, Denmark DK-4000 Mass Spectrometry of Nitro and Nitroso Compounds H. K. Chagger University of Leeds, Department of Fuel and Energy, Leeds, UK LS29JT Environmental Aspects of Compounds Containing Nitro, Nitroso and Amino Groups

Yuan L. Chow Simon Fraser University, Department of Chemistry, Burnaby, British Columbia, Canada V5A 1S6 Photochemistry of Amines and Amino Compounds Photochemistry of Nitro and Nitroso Compounds Helge Egsgaard Risø; National Laboratory, Environmental Science and Technology Department, Roskilde, Denmark DK-4000 Mass Spectrometry of Nitro and Nitroso Compounds P. Eyer Ludwig-Maximilians-Universität München, Walther-Straub-Institut für Pharmakologie und Toxikologie, Nuβbaumstr. 26, München, Germany D-80336 Reactions of Nitrosoarenes with SH Groups Luciano Forlani Dipartimento di Chimica Organica `A. Mangini', viale Risorgimento 4, Bologna, Italy 40136- Hydrogen Bonding and Complex Formation Involving Compounds with Amino, Nitroso and Nitro Groups Albert J. Fry Wesleyan University, Middletown, CT, USA The Electrochemistry of Nitro, Nitroso, and Related Compounds D. Gallemann Ludwig-Maximilians-Universität München, Walther-Straub-Institut für Pharmakologie und Toxikologie, Nuβbaumstr. 26, München, Germany D-80336 Reactions of Nitrosoarenes with SH Groups Tong-Ing Ho National Taiwan University, Department of Chemistry, Roosevelt Road Section 4, Taipei, Taiwan (ROC) Photochemistry of Amines and Amino Compounds Photochemistry of Nitro and Nitroso Compounds William M Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland DD1 4HN

Radiation Chemistry of Amines, Nitro and Nitroso Compounds Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 Wilkens Avenue, Baltimore, MA 21228-5398, USA Thermochemistry Alan H. Mehler Howard University, Department of Biochemistry and Molecular Biology, Washington, DC, USA Nitric Oxide from Arginine: A Biological Surprise Christiana A. Mitsopoulou University of Athens, Department of Chemistry, Athens, Greece 15771 NMR of Compounds Containing –NH2, –NO2 and –NO Groups Norma S. Nudelman Universidad de Buenos Aires, Ciudad Universitaria, Facultad de Ciencias Exactas y Naturales, 1428 Buenos Aires, Argentina SNAr Reactions of Amines in Aprotic Solvents Paul Rademacher Institut für Organische Chemie der Universität Essen, D-45117 Essen, Germany Photoelectron Spectra of Amines, Nitroso and Nitro Compounds Edward W. Randall Queen Mary and Westfield College, Department of Chemistry, London, UK NMR of Compounds Containing –NH2, –NO2 and –NO Groups J. P. B. Sandall University of Exeter, Department of Chemistry, Stocker Road, Exeter, UK EX4 4QD Displacement and ipso-Substitution in Nitration Hanoch Senderowitz Columbia University, Department of Chemistry, New York, NY 10027, USA Molecular Mechanics Calculations John Shorter University of Hull, School of Chemistry, Hull, UK HU6 7RX Electronic Effects of Nitro, Nitroso, Amino and Related Groups

Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry Howard E. Smith Vanderbilt University, Department of Chemistry, Nashville, TN 37235, USA Chiroptical Properties of Amino Compounds Salvatore Sorriso Università di Perugia, Dipartimento di Chimica, Laboratorio di Chimica Fisica, Perugia, Italy 06100 Structural Chemistry Kenneth C. Westaway Laurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6 The Synthesis and Uses of Isotopically Labelled Amino and Quaternary Ammonium Salts A. Williams University of Leeds, Department of Fuel and Energy, Leeds, UK LS29JT Environmental Aspects of Compounds Containing Nitro, Nitroso and Amino Groups D. Lyn H. Williams University of Durham, Chemistry Department, Durham, UK Rearrangement Reactions Involving the Amino, Nitro and Nitroso Groups S- Nitroso Compounds, Formation, Reactions and Biological Activity Jacob Zabicky Ben-Gurion University of the Negev, Institutes for Applied Research, Department of Chemistry, Beer-Sheva, Israel Analytical Aspects of Amino, Quaternary Ammonium, Nitro, Nitroso and Related Functional Groups Heinrich Zollinger Technisch-Chemisches Laboratorium, Eidgenössische Technische Hochschule (ETH), Zürich, Switzerland

Diazotization of Amines and Dediazoniation of Diazonium Ions

Organophosphorus Compounds (1996) R. M. Black Porton Down, Chemical and Biological Defence Establishment, Wiltshire, Salisbury, UK SP4 OJQ The Chemistry of Organophosphorus Chemical Warfare Agents Eli Breuer The Hebrew University of Jerusalem, The School of Pharmacy, Department of Pharmaceutical Chemistry, PO Box 12065, Jerusalem, Israel 91120 Acylphosphonates and their Derivatives O Dahl University of Copenhagen, Department of Chemistry, The H. C. Ørsted Institute, Universitetsparken 5, Copenhagen, Denmark DK-2100 The Preparation and Properties of Tervalent Phosphorus Acid Derivatives R. S. Edmundson Wentworth Avenue, Leeds, UK LS17 7TN Properties and Reactions of Phosphonic and Phosphinic Acids and their Derivatives The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part A: Halo, Hydroxy, Epoxy, Mercapto, Carboxy and Oxo Functionalized Acids The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part B: Diazo, Nitro and Amino Functionalized Acids The Synthesis of Phosphonic and Phosphinic Acids and their Derivatives: Non-Functionalized Acids The Synthesis and Reactions of Thio- and Seleno-Phosphonic and -Phosphinic Acids J. M. Harrison

Porton Down, Chemical and Biological Defence Establishment, Wiltshire, Salisbury, UK SP4 OJQ The Chemistry of Organophosphorus Chemical Warfare Agents Asher Kalir Tel Aviv University, Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv, Israel 69978 Biological Activity of Phosphonic and Phosphinic Acids Henry H. Kalir University of Medicine and Dentistry of New Jersey, Department of Psychiatry, New Jersey Medical School, University Heights, Newark, NJ 07103-2714, USA Biological Activity of Phosphonic and Phosphinic Acids Richard A. J. O'Hair Kansas State University, Department of Chemistry, Willard Hall, Manhattan, KS 66506-3701, USA Gas-Phase Positive and Negative Ion Chemistry of Organophosphorus Compounds via Mass Spectrometric Techniques

Dienes and Polyenes (1997) Zeev Aizenshtat The Hebrew University of Jerusalem, Jerusalem, Casali Institute for Applied Chemistry and Department of Organic Chemistry, Jerusalem, Israel 91904 Analysis of Dienes and Polyenes and Their Structure Determination Zeev B. Alfassi Ben Gurion University, Department of Nuclear Engineering, Beer Sheva, Israel 84102 Radiation Chemistry of Dienes and Polyenes Jan-E. Bäckvall University of Uppsala, Department of Organic Chemistry, Box 531, Uppsala, Sweden S-751 21 Palladium-Catalyzed Oxidation of Dienes

Thomas Bally Université de Fribourg, Institut de Chimie Physique, Pérolles, Fribourg, Switzerland CH-1700 Electronic Structure of Diene and Polyene Radical Cations Lorenzo di Bari Centro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126 Conformation and Chiroptical Properties of Dienes and Polyenes Jordi Benet-Buchholz Universität Essen, Institut für Anorganische Chemie, Universitätsstrasse 3–5, Essen, Germany D-45117 Structural Chemistry of Dienes and Polyenes J. Bertrán Universitat Autònoma de Barcelona, Departament de Química, Bellaterra, Spain 08193 Contribution of Quantum Chemistry to the Study of Dienes and Polyenes Roland Boese Universität Essen, Institut für Anorganische Chemie, Universitätsstrasse 3–5, Essen, Germany D-45117 Structural Chemistry of Dienes and Polyenes Gerhard V. Boyd The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 Intramolecular Cyclization of Dienes and Polyenes V. Branchadell Universitat Autònoma de Barcelona, Departament de Química, Bellaterra, Spain 08193 Contribution of Quantum Chemistry to the Study of Dienes and Polyenes Marvin Charton School of Liberal Arts and Sciences, Chemistry Department, Pratt Institute, Brooklyn, NY11205, USA

Structural Effects on Dienes and Polyenes Matthias K. Diedrich Universität Gesamthochschule Essen, Institut für Organische Chemie, Essen, Germany D-45117 The Effect of Pressure on Reactions of Dienes and Polyenes Yukio Furukawa Department of Chemistry, School of Science, The University of Tokyo, Bunkyo-ku Tokyo, Japan 113 Ultraviolet/Visible, Infrared and Raman Spectra Thomas Haumann Universität Essen, Institut für Anorganische Chemie, Universitätsstrasse 3–5, Essen, Germany D-45117 Structural Chemistry of Dienes and Polyenes Edgar Heilbronner Grütstrasse 10, Herrliberg, Switzerland CH-8704 Electronic Structure of Diene and Polyene Radical Cations Henning Hopf Technical University of Braunschweig, Institut für Organische Chemie, Hagenring 30, Braunschweig, Germany D-38106 Synthesis and Transformation of Radialenes Marianna Kańska University of Warsaw, Department of Chemistry, Poland Syntheses and Uses of Isotopically Labelled Dienes and Polyenes Shigenori Kashimura Kin-ki University, Higashi-Osaka, Japan 577 The Electrochemistry of Dienes and Polyenes Alexander M. Khenkin The Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Graduate School of Applied Science, Jerusalem, Israel 91904

Oxidation of Dienes and Polyenes Kathleen V. Kilway University of California, Department of Chemistry, 94720-1460, Berkeley, CA, USA Acidity of Alkenes and Polyenes Naoki Kise Tottori University, Tottori, Japan 680 The Electrochemistry of Dienes and Polyenes Frank-Gerrit Klärner Universität Gesamthochschule Essen, Institut für Organische Chemie, Essen, Germany D-45117 The Effect of Pressure on Reactions of Dienes and Polyenes Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, , 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry Gerhard Maas University of Ulm, Abteilung Organische Chemie I, Albert-Einstein-Allee 11, Ulm, Germany D-89069 Synthesis and Transformation of Radialenes Goverdhan Mehta University of Hyderabad, Molecular Design and Synthesis Unit of JNCASR and School of Chemistry, Hyderabad, India 500 046 Synthesis of Conjugated Dienes and Polyenes Ronny Neumann The Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Graduate School of Applied Science, Jerusalem, Israel 91904 Oxidation of Dienes and Polyenes John M. Nuss Chiron Corporation, 4560 Horton Street, Emeryville, CA 94608, USA

The Photochemistry of Dienes and Polyenes: Application to the Synthesis of Complex Molecules A. Oliva Universitat Autònoma de Barcelona, Departament de Química, Bellaterra, Spain 08193 Contribution of Quantum Chemistry to the Study of Dienes and Polyenes H. Surya Prakash Rao Pondicherry University, Department of Chemistry, Pondicherry, India 605 014 Synthesis of Conjugated Dienes and Polyenes Carlo Rosini Centro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126 Conformation and Chiroptical Properties of Dienes and Polyenes Piero Salvadori Centro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126 Conformation and Chiroptical Properties of Dienes and Polyenes Tatsuya Shono Kin-ki University, Higashi-Osaka, Japan 577 The Electrochemistry of Dienes and Polyenes M. Sodupe Universitat Autònoma de Barcelona, Departament de Química, Bellaterra, Spain 08193 Contribution of Quantum Chemistry to the Study of Dienes and Polyenes Andrew Streitwieser University of California, Department of Chemistry, 94720-1460, Berkeley, CA, USA Acidity of Alkenes and Polyenes L. R. Subramanian Eberhard-Karls-Universität Tübingen, Institut für Organische Chemie, Auf der Morgenstelle 18, Tübingen, Germany D-72076 Allenyl and Polyenyl Cations

Marit Traetteberg Norwegian University of Science and Technology, Department of Chemistry, Trondheim, Norway N-7055 Structural Chemistry of Dienes and Polyenes Frederick G. West University of Utah, Salt Lake City, Department of Chemistry, UT, USA 84112 The Photochemistry of Dienes and Polyenes: Application to the Synthesis of Complex Molecules Mieczysław Zieliński Jagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland Syntheses and Uses of Isotopically Labelled Dienes and Polyenes H. Zipse Technische Universität Berlin, Institut für Organische Chemie, Strasse des 17 Juni: 135, Berlin, Germany D-10623 Radical Addition to Polyenes

Double-bonded Functional Groups (1997) J.-L. M. Abboud C.S.I.C., Instituto de Química Física `Rocasolano', Serrano 119, Madrid, Spain E-28006 The Thiocarbonyl Group R. Alan Aitken University of St. Andrews, School of Chemistry, St. Andrews, Fife, UK KY16 9ST Pyrolysis Involving Compounds with C=C, C=N and C=O Double Bonds Mihály Bartók József Attila University, Department of Organic Chemistry and Organic Catalysis Research Group of the Hungarian Academy of Sciences, Dóm tér 8, Szeged, Hungary H-6720 Epoxidation of C=X Double Bonds

Heterogeneous Catalytic Hydrogenation Harold Basch Bar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900 Heteropolar Double Bonds Daniel J. Berger Virginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061-0212, USA Radical Anions and Radical Cations Derived from Compounds Containing C=C, C=O or C=N Groups Stefan E. Boiadjiev University of Nevada, Department of Chemistry, Reno, NV 89557, USA Chiroptical Properties of Compounds Containing C=O Groups Otto Exner Academy of Sciences of the Czech Republic, Institute of Organic Chemistry and Biochemistry, Prague, Czech Republic Dipole Moments of Compounds Containing Double Bonds Luciano Forlani Dipartimento di Chimica Organica `A. Mangini', viale Risorgimento 4, Bologna, Italy 40136 Complex Formation Involving Compounds with Double-Bonded Functional Groups Albert J. Fry Wesleyan University, Middletown, CT, USA The Electrochemistry of the C=C, C=O and C=N Groups Tino Gäumann Institute of Physical Chemistry, Federal Institute of Technology, Lausanne, Switzerland 1015 Mass Spectra of Double-Bonded Groups Aharon Gedanken

Bar-Ilan University, Ramat-Gan, Israel 52900 The Chiroptical Properties of the Carbon–Carbon Double Bond W. Haase Institut für Physikalische Chemie, Technische Hochschule, Petersenstr. 20, Darmstadt, Germany 64287 Liquid Crystals with X=Y Groups Nizar Haddad Technion—Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000 Photochemistry of Compounds Containing C=C Double Bonds T. Hanemann Institut für Materialforschung III, Forschungszentrum Karlsruhe, Postfach 3640, Karlsruhe, Germany 76021 Liquid Crystals with X=Y Groups Peter Hlavica Ludwig-Maximilians-Universität München, Walther-Straub-Institut für Pharmakologie and Toxikologie, Nussbaumstrasse 26, München, Germany D-80336 N-Oxidative Transformations of C=N Groups as Means of Toxification and Detoxification Jeff Hoyle Nova Scotia Agricultural College, Chemistry and Soil Science Department, Truro, Nova Scotia, Canada B2N 5E3 Some Synthetic Uses of Double-Bonded Functional Groups Tova Hoz Bar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900 Heteropolar Double Bonds K. J. Ivin The Queen's University of Belfast, and 12, St. Michael's Gardens, South Petherton, Somerset, UK TA13 5BD Advances in the Metathesis of Olefins Asher Kalir Tel Aviv University, Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv, Israel 69978 Biological Activity of Organic Compounds Elicited by the Introduction of Double Bonds

Henry H. Kalir Department of Histology and Cell Biology, Sackler Faculty of Medicine, Tel Aviv, Israel 69978 and Ichilov Hospital, Department of Psychiatry Biological Activity of Organic Compounds Elicited by the Introduction of Double Bonds Marianna Kańska Warsaw University, Department of Chemistry, Warsaw, Poland Syntheses and Uses of Isotopically Labelled Compounds Containing C=C, C=O or C=N Groups Thomas M. Klapötke University of Glasgow, Department of Chemistry, University Avenue, Glasgow, UK G12 8QQ Acidity, Basicity and H-Bonding of Double-Bonded Functional Groups: Nitrones, Nitriles and Thiocarbonyls Pavel Kočovský University of Leicester, Department of Chemistry, Leicester, UK LE1 7RH Electrophilic Additions to Double Bonds Michael Lehnerer Ludwig-Maximilians-Universität München, Walther-Straub-Institut für Pharmakologie and Toxikologie, Nussbaumstrasse 26, München, Germany D-80336 N-Oxidative Transformations of C=N Groups as Means of Toxification and Detoxification Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry David A. Lightner University of Nevada, Department of Chemistry, Reno, NV 89557, USA Chiroptical Properties of Compounds Containing C=O Groups O. Mó

Universidad Autónoma de Madrid, Departamento de Química, C-9, Cantoblanco, Madrid, Spain E-28049 The Thiocarbonyl Group M. T. Molina C.S.I.C., Instituto de Química Médica, Juan de la Cierva 3, Madrid, Spain E-28006 The Thiocarbonyl Group Árpád Molnár József Attila University, Department of Organic Chemistry and Organic Catalysis Research Group of the Hungarian Academy of Sciences, Dóm tér 8, Szeged, Hungary H-6720 Heterogeneous Catalytic Hydrogenation R. Notario C.S.I.C., Instituto de Química Física `Rocasolano', Serrano 119, Madrid, Spain E-28006 The Thiocarbonyl Group Claudia M. Rienäcker University of Glasgow, Department of Chemistry, University Avenue, Glasgow, UK G12 8QQ Acidity, Basicity and H-Bonding of Double-Bonded Functional Groups: Nitrones, Nitriles and Thiocarbonyls Jan Sandström Center for Chemistry and Chemical Engineering, University of Lund, Division of Organic Chemistry 1, 124, Lund, Sweden S-221 00 Strained Olefins Gyula Schneider József Attila University, Department of Organic Chemistry, Dóm tér 8, Szeged, Hungary H-6720 Epoxidation of C=X Double Bonds John Shorter University of Hull, School of Chemistry, Hull, UK HU6 7RX Electronic Effects of Groups Containing Carbon–Carbon or Carbon–Oxygen Double Bonds

Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry James M. Tanko Virginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061-0212, USA Radical Anions and Radical Cations Derived from Compounds Containing C=C, C=O or C=N Groups Peter G. Taylor Open University, Chemistry Department, Walton Hall, Milton Keynes, Bucks, UK MK7 6AA Nucleophilic Attack on Compounds Containing C=C, C=O or C=N Groups Andrew W. Thomas University of St. Andrews, School of Chemistry, St. Andrews, Fife, UK KY16 9ST Pyrolysis Involving Compounds with C=C, C=N and C=O Double Bonds Martin Wills University of Warwick, Department of Chemistry, Coventry, UK CV4 7AL Hydrogenation of Compounds Containing C=C, C=O and C=N Bonds M. Yáñez Universidad Autónoma de Madrid, Departamento de Química, C-9, Cantoblanco, Madrid, Spain E-28049 The Thiocarbonyl Group Mieczysław Ziełiński Jagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland; 48-12-34-05-15 Syntheses and Uses of Isotopically Labelled Compounds Containing C=C, C=O or C=N Groups

Hydrazo, Azo and Azoxy Groups (1997) Hussein Y. Afeefy University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry Zeev B. Alfassi Ben Gurion University of the Negev, Department of Nuclear Engineering, Beer Sheva 84102, Israel Radiation Chemistry of Azo and Hydrazo Compounds J.-P Anselme University of Massachusetts at Boston, Boston, MA 02125-3393, USA Radical Reactions of Azo, Hydrazo and Azoxy Compounds Derek V. Banthorpe University College London, Chemistry Department, London, UK Biological Formation and Reactions of Hydrazo, Azo and Azoxy Groups Harold Basch Bar Ilan University, Department of Chemistry, Ramat Gan 52900, Israel Electronic Structure of Hydrazo, Azo and Azoxy Compounds Gerhard V. Boyd The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 Synthesis and Reactions of Hydrazo, Azo and Azoxy Compounds Erwin Buncel Queen's University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6 Rearrangements of Hydrazo, Azoxy and Azo Compounds: Kinetic, Product and Isotope Studies Otakar Červinka Institute of Chemical Technology, Department of Organic Chemistry, 166 28 Prague 6, Czech Republic

Configuration, Conformation and Chiroptical Properties of the Azo, Azoxy and Hydrazo Groups T.-W.D. Chan The Chinese University of Hong Kong, Department of Chemistry, Shatin, N.T., Hong Kong Mass Spectra of Hydrazo, Azo and Azoxy Compounds Robin A. Cox University of Toronto, Department of Chemistry, Toronto, Ontario, Canada M5S 3H6 Rearrangements of Hydrazo, Azoxy and Azo Compounds: Kinetic, Product and Isotope Studies Victor Glezer The Hebrew University of Jerusalem, Division of Environmental Sciences, Fredy and Nadine Herrmann School of Applied Science, Jerusalem, Israel 91904 Safety and Environmental Effects of Azo Compounds Sarina Grinberg Ben-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel 84105 Analytical Aspects of Compounds Containing the Azo, Azoxy and Hydrazino Functional Groups Noëlle Gueguen-simonet Université de Rennes 1, Laboratoire d'Electrochimie moléculaire et macromoléculaire, UMR N˚6510, Campus de Beaulieu, France Cathodic and Anodic Behaviour of Organic Compounds Possessing –N=N– or > N–N < Linkages William M. Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN The Photochemistry of the Hydrazo, Azo and Azoxy Groups Tova Hoz Bar Ilan University, Department of Chemistry, Ramat Gan 52900, Israel Electronic Structure of Hydrazo, Azo and Azoxy Compounds

Thomas M Klapötke University of Glasgow, Department of Chemistry, Glasgow, UK G12 8QQ Acidity, Basicity and Complex Formation Gen Koga Ibaraki University, Mito, Japan 310 Radical Reactions of Azo, Hydrazo and Azoxy Compounds Branka Kovač `Rugjer Boskovic' Institute, Physical Chemistry Division, Zagreb, Croatia 10000 The Photoelectron Spectroscopy of Hydrazo, Azo and Azoxy Compounds Joel F. Liebman University of Maryland Baltimore Country, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry Joan Mason The Open University, Department of Chemistry, Milton Keynes, UK MK7 6AA NMR Spectroscopy of Azo, Azoxy and Hydrazo Compounds S.F. Nelsen University of Wisconsin, Madison, Department of Chemistry, 1101 University Avenue, Madison, WI 53706-1396, USA Information from the ESR, ENDOR and NMR Spectra of Radicals Related to Hydrazo, Azo and Azoxy Compounds Isaac Nir The Hebrew University of Jerusalem, Department of Pharmacology, Faculty of Medicine, Jerusalem, Israel Toxicological and Pharmacotherapeutical Aspects of Azo, Hydrazo and Azoxy Compounds Igor Novak National University of Singapore, Department of Chemistry, Singapore, Singapore 119260

The Photoelectron Spectroscopy of Hydrazo, Azo and Azoxy Compounds John Shorter University of Hull, School of Chemistry, Hull, UK HU6 7RX Electronic Effects of Hydrazo, Azo and Azoxy Groups Jacques Simonet Université de Rennes 1, Laboratoire d'Electrochimie moléculaire et macromoléculaire, UMR N˚6510, Campus de Beaulieu, France Cathodic and Anodic Behaviour of Organic Compounds Possessing –N=N– or > N–N < Linkages Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry S.W. Tam The Open Learning Institute of Hong Kong, Homantin, Kowloon, Hong Kong Mass Spectra of Hydrazo, Azo and Azoxy Compounds John C. Warner University of Massachusetts at Boston, Boston, MA 02125-3393, USA Radical Reactions of Azo, Hydrazo and Azoxy Compounds Jacob Zabicky Ben-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel 84105 Analytical Aspects of Compounds Containing the Azo, Azoxy and Hydrazino Functional Groups

Organic Silicon Compounds (1998) Wataru Ando University of Tsukuba, Department of Chemistry, Ibaraki 305, Tsukuba, Japan

Cyclic Polychalcogenide Compounds with Silicon Highly Reactive Small-Ring Monosilacycles and Medium-Ring Oligosilacycles Organosilicon Derivatives of Fullerenes Yitzhak Apeloig Technion—Israel Institute of Technology, Department of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry, Haifa, Israel 32000 Theoretical Aspects and Quantum Mechanical Calculations of Silaaromatic Compounds Norbert Auner Fachinstitut für Anorganische und Allgemeine Chemie der Humboldt Universität Berlin, Berlin, FRG D 10115 Silicon–Carbon and Silicon–Nitrogen Multiply Bonded Compounds David Avnir The Hebrew University of Jerusalem, Institute of Chemistry, Jerusalem, Israel 91904 Organo-Silica Sol–Gel Materials Alan R. Bassindale The Open University, Department of Chemistry, Milton Keynes, UK MK7 6AA Activating and Directive Effects of Silicon Reaction Mechanisms of Nucleophilic Attack at Silicon Rosa Becerra CSIC, Instituto de Quimica Fisica `Rocasolano', C/Serrano, 119, Madrid, Spain 28006 Thermochemistry Johannes Belzner Institut für Organische Chemie der Georg-August-Universität Göttingen, Tammannstr., Göttingen, Germany 2, D-37077 Alkaline and Alkaline Earth Silyl Compounds—Preparation and Structure

M. B. Boisen Jr Materials Science and Engineering and Mathematics, Departments of Geological Sciences, Virginia Tech, Blacksburg, VA 24061, USA A Molecular Modeling of the Bonded Interactions of Crystalline Silica Mark Botoshansky Technion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000 The Structural Chemistry of Organosilicon Compounds A. G. Brook University of Toronto, Lash Miller Chemical Laboratories, Toronto, Ontario, Canada M5S 3H6 The Photochemistry of Organosilicon Compounds Philip C. Bulman Page Loughborough University, Department of Chemistry, Loughborough, Leicestershire, UK LE11 3TU Acyl Silanes C. Chatgilialoglu Consiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129 Tris(trimethylsilyl)silane in Organic Synthesis Buh-Luen Cheng Institute of Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei, Taiwan, Peoples’ Republic of China 11529 and National Tsing Hua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China 30043 Steric Effects of Silyl Groups Nami Choi University of Tsukuba, Department of Chemistry, Tsukuba, Japan Ibaraki 305 Cyclic Polychalcogenide Compounds with Silicon Ernest W. Colvin University of Glasgow, Department of Chemistry, G12 8QQ, Glasgow, UK Recent Synthetic Applications of Organosilicon Reagents Uwe Dehnert

Institut für Organische Chemie der Georg-August-Universität Göttingen, Tammannstr., Göttingen, Germany 2, D-37077 Alkaline and Alkaline Earth Silyl Compounds—Preparation and Structure Robert Drake Dow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UK CF63 2YL Recent Advances in the Chemistry of Siloxane Polymers and Copolymers Jacques Dubac Université Paul-Sabatier, Hétérochimie Fondamentale et Appliquée (ESA-CNRS 5069), 118, Route de Narbonne, Toulouse Cedex, France 31062 Group 14 Metalloles, Ionic Species and Coordination Compounds Moris S. Eisen Technion—Israel Institute of Technology, Department of Chemistry, Kiryat Hatechnion, Haifa, Israel 32000 Transition-Metal Silyl Complexes C. Ferreri Consiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129 Tris(trimethylsilyl)silane in Organic Synthesis D. A. (`Fred') Armitage King's College London, Department of Chemistry, Strand, London, UK WC2R 2LS Chemistry of Compounds with Silicon–Sulphur, Silicon–Selenium and Silicon–Tellurium Bonds Toshio Fuchigami Tokyo Institute of Technology, Department of Electrochemistry, Midori-ku, Yokohama, Japan 226 Electrochemistry of Organosilicon Compounds Peter P Gaspar Washington University, Department of Chemistry, St. Louis, MI 63130-4899, USA Silylenes G. V. Gibbs

Materials Science and Engineering and Mathematics, Departments of Geological Sciences, Virginia Tech, Blacksburg, VA 24061, USA A Molecular Modeling of the Bonded Interactions of Crystalline Silica T. Gimisis Consiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129 Tris(trimethylsilyl)silane in Organic Synthesis Simon J. Glynn The Open University, Department of Chemistry, Milton Keynes, UK MK7 6AA Activating and Directive Effects of Silicon Reaction Mechanisms of Nucleophilic Attack at Silicon Norman Goldberg Institut für Organische Chemie der Technischen Universität Berlin, Straße des 17 Juni 135, Berlin, Germany D-10623 Gas-Phase Ion Chemistry of Silicon-Containing Molecules Christian Guérin Université Montpellier II, Chimie Moléculaire et Organisation du Solide (UMR-CNRS 5637), Place E. Bataillon, Montpellier Cedex 5, France 34095 Group 14 Metalloles, Ionic Species and Coordination Compounds Edwin Hengge Technical University, Institute of Inorganic Chemistry, Graz, Austria Recent Advances in the Chemistry of Cyclopolysilanes R. Jih-Ru Hwu Institute of Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei, Taiwan, Peoples’ Republic of China 11529 and National Tsing Hua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China 30043 Steric Effects of Silyl Groups Jörg Jung Institut für Organische Chemie der Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58, Giessen, Federal Republic of Germany D-35392

Matrix Isolation Studies of Silicon Compounds Peter Jutzi University of Bielefeld, Faculty of Chemistry, Bielefeld, Germany 33615 Cyclopentadienyl Silicon Compounds Yoshio Kabe University of Tsukuba, Department of Chemistry, Ibaraki 305, Tsukuba, Japan Highly Reactive Small-Ring Monosilacycles and Medium-Ring Oligosilacycles Menahem Kaftory Technion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000 The Structural Chemistry of Organosilicon Compounds Inna Kalikhman Ben-Gurion University of the Negev, Department of Chemistry, Beer Sheva, Israel 84105 Hypervalent Silicon Compounds Moshe Kapon Technion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000 The Structural Chemistry of Organosilicon Compounds Miriam Karni Technion—Israel Institute of Technology, Department of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry, Haifa, Israel 32000 Theoretical Aspects and Quantum Mechanical Calculations of Silaaromatic Compounds Mitsuo Kira Tohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan 980-77 Mechanistic Aspects of the Photochemistry of Organosilicon Compounds Svetlana Kirpichenko Siberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk, Russia 664033 Silatranes and their Tricyclic Analogs Sukhbinder S. Klair

Loughborough University, Department of Chemistry, Loughborough, Leicestershire, UK LE11 3TU Acyl Silanes Lisa C. Klein Rutgers—The State University of New Jersey, Ceramics Department, Piscataway, NJ 08855-0909, USA Organo-Silica Sol–Gel Materials Alla V. Koblik ChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435 Tautomeric Equilibria and Rearrangements Involving Phenols Daniel Kost Ben-Gurion University of the Negev, Department of Chemistry, Beer Sheva, Israel 84105 Hypervalent Silicon Compounds Takahiro Kusukawa University of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305 Organosilicon Derivatives of Fullerenes R. M. Laine University of Michigan, Departments of Materials Science and Engineering and Chemistry, Ann Arbor, MI 48109-2136, USA Si-Containing Ceramic Precursors David Levy Instituto de Ciencia de Materiales de Madrid, C.S.I.C., Cantoblanco, Madrid, Spain 28049 Organo-Silica Sol–Gel Materials Larry N. Lewis GE Corporate Research & Development Center, Schenectady, NY, USA 12309 Recent Advances in the Direct Process Zhaoyang Li State University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA

Recent Advances in the Hydrosilylation and Related Reactions Paul D. Lickiss Imperial College of Science, Department of Chemistry, Technology and Medicine, London, UK SW7 2AY Silicenium Ions—Experimental Aspects Shiuh-Tzung Liu National Taiwan University, Department of Chemistry, Taipei, Taiwan, Peoples’ Republic of China 106 Synthetic Applications of Allylsilanes and Vinylsilanes Tien-Yau Luh National Taiwan University, Department of Chemistry, Taipei, Taiwan, Peoples’ Republic of China 106 Synthetic Applications of Allylsilanes and Vinylsilanes Sergei M. Lukyanov ChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435 Tautomeric Equilibria and Rearrangements Involving Phenols Thomas Müller Humboldt Universität Berlin, Fachinstitut für Anorganische und Analytische Chemie der, Berlin, Germany D-10115 Silicon–Carbon and Silicon–Nitrogen Multiply Bonded Compounds Silyl-Substituted Carbocations Gerhard Maas Universität Ulm, Abteilung Organische Chemie I, Albert-Einstein-Allee 11, Ulm, Germany D-89081 Silicon-Substituted Carbenes Iain MacKinnon Dow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UK CF63 2YL

Recent Advances in the Chemistry of Siloxane Polymers and Copolymers Christoph Maerker The University of Erlangen-Nürnberg, Computer Chemistry Center of the Institute of Organic Chemistry, Henkestrasse 42, Erlangen, Germany 91054 Silicenium Ions: Quantum Chemical Computations Günther Maier Institut für Organische Chemie der Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58, Giessen, Federal Republic of Germany D-35392 Matrix Isolation Studies of Silicon Compounds Michael J. Mckenzie Loughborough University, Department of Chemistry, Loughborough, Leicestershire, UK LE11 3TU Acyl Silanes Andreas Meudt Institut für Organische Chemie der Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58, Giessen, Federal Republic of Germany D-35392 Matrix Isolation Studies of Silicon Compounds Philippe Meunier Université de Bourgogne, Synthèse et Electrosynthèse Organométalliques (UMR-CNRS 5632), 6 Boulevard Gabriel, Dijon Cedex, France 21004 Group 14 Metalloles, Ionic Species and Coordination Compounds Takashi Miyazawa The Institute of Physical and Chemical Research, Photodynamics Research Center, (RIKEN), 19-1399, Koeji, Nagamachi, Aoba-ku, Sendai, Japan 980 Mechanistic Aspects of the Photochemistry of Organosilicon Compounds Shigeru Nagase Tokyo Metropolitan University, Department of Chemistry, Graduate School of Science, Tokyo, Hachioji, Japan 192-03

Polyhedral Silicon Compounds Iwao Ojima State University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA Recent Advances in the Hydrosilylation and Related Reactions Renji Okazaki The University of Tokyo, Department of Chemistry, Graduate School of Science, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan 113 Recent Advances in the Chemistry of Silicon–Heteroatom Multiple Bonds Harald Pacl Institut für Organische Chemie der Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58, Giessen, Federal Republic of Germany D-35392 Matrix Isolation Studies of Silicon Compounds Vadim Pestunovich Siberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk, Russia 664033 Silatranes and their Tricyclic Analogs Paul von Ragué Schleyer The University of Erlangen-Nürnberg, Computer Chemistry Center of the Institute of Organic Chemistry, Henkestrasse 42, Erlangen, Germany 91054 Silicenium Ions: Quantum Chemical Computations Stephen Rosenthal Loughborough University, Department of Chemistry, Loughborough, Leicestershire, UK LE11 3TU Acyl Silanes Hideki Sakurai Science University of Tokyo, Department of Industrial Chemistry, Faculty of Science and Technology, Noda, Chiba, Japan 278

Mechanism and Structures in Alcohol Addition Reactions of Disilenes and Silenes Ulrich Schubert the Technical University of Vienna, Institute for Inorganic Chemistry, Vienna, Austria A-1060 Organo-Silica Sol–Gel Materials Helmut Schwarz Institut für Organische Chemie der Technischen Universität Berlin, Straße des 17 Juni 135, Berlin, Germany D-10623 Gas-Phase Ion Chemistry of Silicon-Containing Molecules Akira Sekiguchi University of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305 Polyhedral Silicon Compounds A. Sellinger University of New Mexico, Sandia National Laboratory, Advanced Materials Laboratory, 1001 University Blvd. S.E., Albuquerque, NM 87106, USA Si-Containing Ceramic Precursors Hans-Ullrich Siehl Universität Ulm, Abteilung für Organische Chemie I der, Ulm, Germany D-86069 Silyl-Substituted Carbocations Harald Stüger Technical University, Institute of Inorganic Chemistry, Graz, Austria Recent Advances in the Chemistry of Cyclopolysilanes Reinhold Tacke Universität Würzburg, Institut für Anorganische Chemie, Am Hubland, Würzburg, Germany D-97074 Chirality in Bioorganosilicon Chemistry Toshio Takayama Kanagawa University, Department of Applied Chemistry, Faculty of Engineering, 3-27-1 Rokkakubashi, Yokohama, Japan 221

29Si NMR Spectroscopy of Organosilicon Compounds Yoshito Takeuchi Kanagawa University, Department of Chemistry, Faculty of Science, 2946 Tsuchiya, Hiratsuka, Japan 259-12 29Si NMR Spectroscopy of Organosilicon Compounds Peter G. Taylor The Open University, Department of Chemistry, Milton Keynes, UK MK7 6AA Activating and Directive Effects of Silicon Reaction Mechanisms of Nucleophilic Attack at Silicon Richard Taylor Dow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UK CF63 2YL Recent Advances in the Chemistry of Siloxane Polymers and Copolymers Norihiro Tokitoh The University of Tokyo, Department of Chemistry, Graduate School of Science, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan 113 Recent Advances in the Chemistry of Silicon–Heteroatom Multiple Bonds Shwu-Chen Tsay Institute of Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei, Taiwan, Peoples’ Republic of China 11529 and National Tsing Hua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China 30043 Steric Effects of Silyl Groups Mikhail Voronkov Siberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk, Russia 664033 Silatranes and their Tricyclic Analogs Stephan A. Wagner

Universität Würzburg, Institut für Anorganische Chemie, Am Hubland, Würzburg, Germany D-97074 Chirality in Bioorganosilicon Chemistry Robin Walsh University of Reading, Department of Chemistry, PO Box 224, Whiteknights, Reading, UK RG6 6AD Thermochemistry Robert West University of Wisconsin at Madison, Department of Chemistry, Madison, WI 53706, USA Silylenes Anna B. Wojcik Rutgers—The State University of New Jersey, Ceramics Department, Piscataway, NJ 08855-0909, USA Organo-Silica Sol–Gel Materials Jiawang Zhu State University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA Recent Advances in the Hydrosilylation and Related Reactions Wolfgang Ziche Fachinstitut für Anorganische und Allgemeine Chemie der Humboldt Universität Berlin, Berlin, FRG D 10115 Silicon–Carbon and Silicon–Nitrogen Multiply Bonded Compounds

Organic Derivatives of Gold and Silver (1999) R. Alan Aitken University of St. Andrews, School of Chemistry, St. Andrews, Fife, UK KY16 9ST Pyrolysis of Organic Derivatives of Silver and Gold Harold Basch Bar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900

General and Theoretical Aspects of Organic Gold Compounds Angela Bayler Technische Universität München, Lehrstuhl für Anorganische und Analytische Chemie, Garching, Germany D-85747 Synthesis and Uses of Organosilver Compounds Alice E. Bruce University of Maine, Department of Chemistry, Orono, ME 04469-5706, USA The Electrochemistry of Gold and Silver Complexes Mitchell R. M. Bruce University of Maine, Department of Chemistry, Orono, ME 04469-5706, USA The Electrochemistry of Gold and Silver Complexes Victor Chechik University of Sheffield, Department of Chemistry, Sheffield, UK S3 7HF Gold–Thiol Self-Assembled Monolayers John P. Fackler Jr. Texas A&M University, Department of Chemistry, College Station, TX 77843-3012, USA Rearrangement of Gold and Silver Complexes C Frank Shaw III University of Wisconsin-Milwaukee, Department of Chemistry, P O Box 413, Milwaukee, WI 53201-0413, USA NMR and ESR Spectroscopy Applied to Gold and Silver Compounds Simon P. Fricker AnorMED Inc., #100 20353-64th Avenue, Langley, British Columbia, Canada V2Y 1N5 Medicinal Chemistry of Gold Compounds Sarina Grinberg Ben-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel Analytical Aspects of Organogold and Organosilver Compounds

Andreas Grohmann Technische Universität München, Lehrstuhl für Anorganische und Analytische Chemie, Garching, Germany D-85747 Synthesis and Uses of Organogold Compounds William M. Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland DD1 4HN The Organic Photochemistry of Silver and Gold Tova Hoz Bar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900 General and Theoretical Aspects of Organic Gold Compounds Marianna Kańska University of Warsaw, Department of Chemistry, Warsaw, Poland Syntheses and Uses of Isotopically Labelled Compounds of Silver and Gold Ryszard Kański University of Warsaw, Department of Chemistry, Warsaw, Poland Syntheses and Uses of Isotopically Labelled Compounds of Silver and Gold Thomas M. Klapötke University of Munich (LMU), Institute of Inorganic Chemistry, Meiserstrasse 1, D-80333 Munich, Germany Acidity, Basicity and H Bonds Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry of the Organometallic Compounds of Silver and Gold Ahmed A. Mohamed University of Maine, Department of Chemistry, Orono, ME 04469-5706, USA The Electrochemistry of Gold and Silver Complexes Igor Novak

National University of Singapore, Department of Chemistry, Singapore, Singapore 119260 The Photoelectron Spectroscopy of Organic Derivatives of Gold and Silver M. Elena Olmos Technische Universität München, Lehrstuhl für Anorganische und Analytische Chemie, Garching, Germany D-85747 Synthesis and Uses of Organogold Compounds R. V. Parish UMIST, Department of Chemistry, PO Box 88, Manchester, UK M60 1QD Mössbauer Spectroscopy with Gold Compounds Annette Schier Technische Universität München, Lehrstuhl für Anorganische und Analytische Chemie, Garching, Germany D-85747 Synthesis and Uses of Organogold Compounds Hubert Schmidbaur Technische Universität München, Lehrstuhl für Anorganische und Analytische Chemie, Garching, Germany D-85747 Synthesis and Uses of Organogold Compounds Synthesis and Uses of Organosilver Compounds José Martinho Simões Universidade de Lisboa, Departamento de Química e Bioquímica and CiTecMat, Faculdade de Ciências, 1700 Lisboa, Portugal Thermochemistry of the Organometallic Compounds of Silver and Gold Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry of the Organometallic Compounds of Silver and Gold Charles J. M. Stirling University of Sheffield, Department of Chemistry, Sheffield, UK S3 7HF

Gold–Thiol Self-Assembled Monolayers Suning Wang Queen's University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6 Rearrangement of Gold and Silver Complexes Jacob Zabicky Ben-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel Analytical Aspects of Organogold and Organosilver Compounds MieczysŁaw Zieliński Jagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland Syntheses and Uses of Isotopically Labelled Compounds of Silver and Gold

Dienes and Polyenes (2000) Patrick H Beusker University of Nijmegen, Department of Organic Chemistry, NSR Center for Molecular Structure, Design and Synthesis, Toernooiveld, Nijmegen, ED, The Netherlands 6525 Intermolecular Cyclization Reactions to form Carbocycles Gerhard V. Boyd The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 Cycloaddition to Give Heterocycles Cinzia Chiappe Università di Pisa, Dipartimento di Chimica Bioorganica e Biofarmacia, Via Bonanno 33, Pisa, Italy 56126 Electrophilic Additions to Dienes and Polyenes Kimberly A. Conlon State University of New York at Stony Brook, Department of Pharmacological Sciences, School of Medicine, Stony Brook, NY 11794-8651, USA Synthetic Applications of Dienes and Polyenes, Excluding Cycloadditions Bruce H. O. Cook

McMaster University, Department of Chemistry, 1280 Main St. W., Hamilton, Ontario, Canada L8S 4M1 Photopericyclic Reactions of Conjugated Dienes and Trienes William A. Donaldson Marquette University, Department of Chemistry, P. O. Box 1881, Milwaukee, WI 53201-1881, USA Organometallic Complexes of Dienes and Polyenes G. Farkas Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes K. Fodor Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes Á. Fürcht Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes L. Hegedüs Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes William M. Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN Photochemistry of Non-Conjugated Dienes Zs. P. Karancsi Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes

Alla V. Koblik Rostov State University, Institute of Physical and Organic Chemistry, Stachki str., 194/2, Rostov on Don, Russia 344104 Rearrangements of Dienes and Polyenes Norbert Krause University of Dortmund, Organic Chemistry II, Dortmund, Germany D-44221 Nucleophilic Additions to Dienes, Enynes and Polyenes Dietmar Kuck Universität Bielefeld, Fakultät für Chemie, Universitätsstraße 25, Bielefeld, Germany D-33615 and Universität-Gesamthochschule Paderborn, Germany and Fachbereich Chemie und Chemietechnik, Warburger Straße 100, Paderborn, Germany D-33098 Mass Spectrometry and Gas-Phase Ion Chemistry of Dienes and Polyenes William J. Leigh McMaster University, Department of Chemistry, 1280 Main St. W., Hamilton, Ontario, Canada L8S 4M1 Photopericyclic Reactions of Conjugated Dienes and Trienes Sergei M. Lukyanov Rostov State University, Institute of Physical and Organic Chemistry, Stachki str., 194/2, Rostov on Don, Russia 344104 Rearrangements of Dienes and Polyenes Michael Mormann Universität-Gesamthochschule Paderborn, Fachbereich Chemie und Chemietechnik, Warburger Straße 100, Paderborn, Germany D-33098 Mass Spectrometry and Gas-Phase Ion Chemistry of Dienes and Polyenes Marie-Françoise Ruasse l'Université Paris 7-Denis Diderot, Institut de Topologie et de Dynamique des Systèmes de, associé au CNRS, UPRESA 7086, 1, rue Guy de la Brosse, Paris, France 75005 Electrophilic Additions to Dienes and Polyenes Hans W Scheeren

University of Nijmegen, Department of Organic Chemistry, NSR Center for Molecular Structure, Design and Synthesis, Toernooiveld, Nijmegen, ED, The Netherlands 6525 Intermolecular Cyclization Reactions to form Carbocycles Peter R. Schreiner Georg-August Universität Göttingen, Institute für Organische Chemie, Tammannstr. 2, Göttingen, Germany D-37077 Catalysis of Diels–Alder Reactions in Water and in Hydrogen-Bonding Environments Toshio Takayama Kanagawa University, Department of Applied Chemistry, Faculty of Engineering, 3-27-1 Rokkakubashi, Yokohama, Japan 221-8686 NMR Spectroscopy of Dienes and Polyenes Yoshito Takeuchi Kanagawa University, Department of Chemistry, Faculty of Science, 2946 Tsuchiya, Hiratsuka, Japan 259-1293 NMR Spectroscopy of Dienes and Polyenes A. Tungler Technical University of Budapest, Department of Chemical Technology, Budafoki út 8, Budapest, Hungary H-1521 Reduction of Dienes and Polyenes Nanette Wachter-Jurcsak Hofstra University, Department of Chemistry, Biochemistry and Natural Science, Hempstead, NY 11549-1090, USA Synthetic Applications of Dienes and Polyenes, Excluding Cycloadditions Alexander Wittkopp Georg-August Universität Göttingen, Institute für Organische Chemie, Tammannstr. 2, Göttingen, Germany D-37077 Catalysis of Diels–Alder Reactions in Water and in Hydrogen-Bonding Environments Claudia Zelder University of Dortmund, Organic Chemistry II, Dortmund, Germany D-44221

Nucleophilic Additions to Dienes, Enynes and Polyenes

Organic Silicon Compounds (2001) Yitzhak Apeloig Technion-Israel Institute of Technology, Department of Chemistry, and the Lise Meitner Minerva, 32000, Haifa, Israel Theoretical Aspects of Compounds Containing Si, Ge, Sn and Pb H. Bock Johann Wolfgang Goethe University, Institute of Inorganic Chemistry, Marie-Curie Street 11, Frankfurt am Main, Germany D-60439 (Helium I)-Photoelectron Spectra of Silicon Compounds: History and Achievements Concerning their Molecular States Bruno Boury Université de Montpellier II, Laboratoire de Chimie Moléculaire et Organisation du Solide UMR 5637, CC007, Place E. Bataillon, Montpellier cedex, France 34095 Nanostructured Hybrid Organic–Inorganic Solids from Molecules to Materials C. Chatgilialoglu Consiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129 Silyl Radicals Cheol Ho Choi Iowa State University, Department of Chemistry, Ames, IA 50011, USA Chemistry on Silicon Surfaces Robert J. P. Corriu Université de Montpellier II, Laboratoire de Chimie Moléculaire et Organisation du Solide UMR 5637, CC007, Place E. Bataillon, Montpellier cedex, France 34095 Nanostructured Hybrid Organic–Inorganic Solids from Molecules to Materials Simonetta Fornarini Università di Roma ``La Sapienza'', Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, P.le A. Moro 5, Roma, Italy I-00185

Ion–Molecule Reactions of Silicon Cations Mark S Gordon Iowa State University, Department of Chemistry, Ames, IA 50011, USA Chemistry on Silicon Surfaces Uwe Herzog Institute of Inorganic Chemistry, Freiberg University of Mining and Technology, Leipziger Str. 29, Freiberg, Germany D-09596 Organosilicon Halides—Synthesis and Properties Takeaki Iwamoto Tohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan 980–8578 Silyl Migrations Bettina Jaschke University of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077 Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen Bonds Jürgen Kapp The University of Erlangen-Nürnberg, Computer Chemistry Center of the Institute of Organic Chemistry, Henkestrasse 42, Erlangen, Germany 91054 Theoretical Aspects of Compounds Containing Si, Ge, Sn and Pb Miriam Karni Technion-Israel Institute of Technology, Department of Chemistry, and the Lise Meitner Minerva, 32000, Haifa, Israel Theoretical Aspects of Compounds Containing Si, Ge, Sn and Pb Mitsuo Kira Tohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan 980–8578 Silyl Migrations Uwe Klingebiel University of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077 Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen Bonds William J. Leigh

McMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 Kinetic Studies of the Reactions of Si=C and Si=Si Bonds Paul D Lickiss Imperial College of Science Technology and Medicine, Department of Chemistry, London, England SW7 2AY Polysilanols Tracy L. Morkin McMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 Kinetic Studies of the Reactions of Si=C and Si=Si Bonds Daniel E. Morse University of California, Marine Biotechnology Center and Department of Molecular, Cellular and Developmental Biology, Santa Barbara, CA 93106, USA Biotechnology Reveals New Routes to Synthesis and Structural Control of Silica and Polysilsesquioxanes Peter Neugebauer University of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077 Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen Bonds Thomas R. Owens McMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 Kinetic Studies of the Reactions of Si=C and Si=Si Bonds C.H. Schiesser The University of Melbourne, Victoria, School of Chemistry, Victoria, Australia 3010 Silyl Radicals Paul von R. Schleyer The University of Erlangen-Nürnberg, Computer Chemistry Center of the Institute of Organic Chemistry, Henkestrasse 42, Erlangen, Germany 91054 Theoretical Aspects of Compounds Containing Si, Ge, Sn and Pb

Jan Schraml Institute of Chemical Process Fundamentals, Academy of Sciences of the Czech Republic, Prague, Czech Republic 165 02 29Si NMR Experiments in Solutions of Organosilicon Compounds B. Solouki Johann Wolfgang Goethe University, Institute of Inorganic Chemistry, Marie-Curie Street 11, Frankfurt am Main, Germany D-60439 (Helium I)-Photoelectron Spectra of Silicon Compounds: History and Achievements Concerning their Molecular States David Y Son Southern Methodist University, Department of Chemistry, P.O. Box 750314, Dallas, TX, USA Silicon-Based Dendrimers and Hyperbranched Polymers Kohei Tamao Kyoto University, Institute for Chemical Research, Uji, Kyoto, Japan 611-0011 Polysiloles and Related Silole-Containing Polymers Kozo Toyota Tohoku University, Department of Chemistry, Graduate School of Science, Aoba-ku, Sendai, Japan 980-8578 Synthesis of Multiply Bonded Phosphorus Compounds Using Silylphosphines and Silylphosphides Manfred Weidenbruch Universität Oldenburg, Fachbereich Chemie, Oldenburg, Germany D-26111 Recent Advances in the Chemistry of Silicon–Silicon Multiple Bonds Robert West University of Wisconsin, Organosilicon Research Center, Department of Chemistry, Madison, WI 53706, USA Polysilanes: Conformations, Chromotropism and Conductivity Shigehiro Yamaguchi Kyoto University, Institute for Chemical Research, Uji, Kyoto, Japan 611-0011 Polysiloles and Related Silole-Containing Polymers

Masaaki Yoshifuji Tohoku University, Department of Chemistry, Graduate School of Science, Aoba-ku, Sendai, Japan 980-8578 Synthesis of Multiply Bonded Phosphorus Compounds Using Silylphosphines and Silylphosphides

Organic Germanium, Tin and Lead Compounds (2003) Klavdiya A. Abzaeva A. E. Favorsky Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str, Irkutsk, Russia 664033 Genesis and Evolution in the Chemistry of Organogermanium, Organotin and Organolead Compounds Yuri I. Baukov Russian State Medical University, Department of General and Bioorganic Chemistry, 1 Ostrovityanov St, Moscow, Russia 117997 Hypervalent Compounds of Organic Germanium, Tin and Lead Derivatives Sergey E. Boganov N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47, Moscow, Russian Federation 119991 Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenes and Plumbylenes Michael W. Carland The University of Melbourne, School of Chemistry, Melbourne, Victoria, Australia 3010 Synthetic Uses of R3MH (M = Ge, Sn, Pb) Annie Castel Université Paul Sabatier, Laboratoire d'Hétérochimie Fondamentale et Appliquée, UMR 5069 du CNRS, Toulouse cedex, France 31062 Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure and Reactivity

Marvin Charton School of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA Structural Effects on Germanium, Tin and Lead Compounds Alexey N. Egorochkin G. A. Razuvaev Institute of Metallorganic Chemistry of the Russian Academy of Sciences, 49 Tropinin Str., Nizhny Novgorod, Russia 603950 Similarities and Differences of Organic Compounds of Germanium, Tin and Lead Mikhail P. Egorov N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47, Moscow, Russian Federation 119991 Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenes and Plumbylenes Valery I. Faustov N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47, Moscow, Russian Federation 119991 Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenes and Plumbylenes Eric Fouquet Université Bordeaux I, Laboratoire de Chimie Organique et Organométallique, 351, Cours de la Liberation, Talence Cedex, France 33405 Synthetic Applications of Organic Germanium, Tin and Lead Compounds (Excluding R3MH) Gernot Frenking Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032 Theoretical Studies of Organic Germanium, Tin and Lead Compounds Inga Ganzer Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032 Theoretical Studies of Organic Germanium, Tin and Lead Compounds Ionel Haiduc

University of Texas at El Paso, Department of Chemistry, El Paso, TX 79968, USA Transition Metal Complexes of Germanium, Tin and Lead Michael Hartmann Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032 Theoretical Studies of Organic Germanium, Tin and Lead Compounds Luba Ignatovich Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006 Biological Activity of Organogermanium Compounds Klaus Jurkschat Lehrstuhl für Anorganische Chemie II der Universität Dortmund, Dortmund, Germany D-44221 Organometallic Polymers of Germanium, Tin and Lead Thomas M. Klapötke Ludwig-Maximilians-University Munich, Department of Chemistry, Butenandtstr. 5-13 (Building D), Munich, Germany D-81377 Recent Advances in Acidity, Complexing, Basicity and H-Bonding of Organo Germanium, Tin and Lead Compounds Karl W Klinkhammer University of Stuttgart, Institute for Inorganic Chemistry, Pfaffenwaldring 55, Stuttgart, Germany D-70569 Recent Advances in Structural Chemistry of Organic Germanium, Tin and Lead Compounds Stanislav Kolesnikov N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect, Moscow, Russian Federation 119991 Trichlorogermane, a New Superacid in Organic Chemistry Alexander I. Kruppa Institute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090 Radical Reaction Mechanisms of and at Organic Germanium, Tin and Lead Vladimir Ya. Lee University of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305-8571

Cage Compounds of Heavier Group 14 Elements Unsaturated Three-Membered Rings of Heavier Group 14 Elements Tatyana V. Leshina Institute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090 Radical Reaction Mechanisms of and at Organic Germanium, Tin and Lead Conor Long School of Chemical Sciences, Dublin City University, Dublin 9, Ireland The Photochemistry of Organometallic Compounds of Germanium, Tin and Lead Edmunds Lukevics Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006 Biological Activity of Organogermanium Compounds Biological Activity of Organotin and Organolead Compounds Heinrich Chr. Marsmann Universität Paderborn, Fachbereich Chemie, Anorganische Chemie, Warburger Straße 100, Paderborn, Germany D-30095 Further Advances in Germanium, Tin and Lead NMR Michael Mehring Lehrstuhl für Anorganische Chemie II der Universität Dortmund, Dortmund, Germany D-44221 Organometallic Polymers of Germanium, Tin and Lead Josef Michl University of Colorado, Department of Chemistry and Biochemistry, Boulder, CO 80309-0215, USA Free and Complexed R3M+ Cations (M = Ge, Sn, Pb) Oleg M. Nefedov N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect, Moscow, Russian Federation 119991 Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenes and Plumbylenes

Trichlorogermane, a New Superacid in Organic Chemistry Renji Okazaki Japan Women's University, Department of Chemical and Biological Sciences, Faculty of Science, 2-8-1 Mejirodai, Bunkyo-ku, Tokyo, Japan 112–8681 Multiply Bonded Germanium, Tin and Lead Compounds Keith H. Pannell University of Texas at El Paso El Paso, Department of Chemistry, TX 79968, USA Transition Metal Complexes of Germanium, Tin and Lead Mary T. Pryce School of Chemical Sciences, Dublin City University, Dublin 9, Ireland The Photochemistry of Organometallic Compounds of Germanium, Tin and Lead Olga Pudova Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006 Biological Activity of Organotin and Organolead Compounds Claudia M. Rienäcker Ludwig-Maximilians-University Munich, Department of Chemistry, Butenandtstr. 5-13 (Building D), Munich, Germany D-81377 Recent Advances in Acidity, Complexing, Basicity and H-Bonding of Organo Germanium, Tin and Lead Compounds José M. Riveros University of São Paulo, Institute of Chemistry, Caixa Postal 26077, São Paulo, Brazil CEP 05513-970 Gas-Phase Chemistry and Mass Spectrometry of Ge-, Sn- and Pb-Containing Compounds Pierre Riviere Université Paul Sabatier, Laboratoire d'Hétérochimie Fondamentale et Appliquée, UMR 5069 du CNRS, Toulouse cedex, France 31062 Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure and Reactivity Monique Riviere-Baudet

Université Paul Sabatier, Laboratoire d'Hétérochimie Fondamentale et Appliquée, UMR 5069 du CNRS, Toulouse cedex, France 31062 Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure and Reactivity Carl H. Schiesser The University of Melbourne, School of Chemistry, Melbourne, Victoria, Australia 3010 Synthetic Uses of R3MH (M = Ge, Sn, Pb) Akira Sekiguchi University of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305-8571 Cage Compounds of Heavier Group 14 Elements Unsaturated Three-Membered Rings of Heavier Group 14 Elements Hemant K. Sharma University of Texas at El Paso, Department of Chemistry, El Paso, TX 79968, USA Transition Metal Complexes of Germanium, Tin and Lead Keiko Takashima University of Londrina, Department of Chemistry, Caixa Postal 6001, Londrina, PR, Brazil CEP 86051-970 Gas-Phase Chemistry and Mass Spectrometry of Ge-, Sn- and Pb-Containing Compounds Stanislav N. Tandura N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect, Moscow, Russia 119991 Hypervalent Compounds of Organic Germanium, Tin and Lead Derivatives Trichlorogermane, a New Superacid in Organic Chemistry Marc B. Taraban Institute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090 Radical Reaction Mechanisms of and at Organic Germanium, Tin and Lead Norihiro Tokitoh

Kyoto University, Institute for Chemical Research, Gokasho, Uji, Kyoto, Japan 611-0011 Multiply Bonded Germanium, Tin and Lead Compounds Frank Uhlig Universität Dortmund, Fachbereich Chemie, Anorganische Chemie II, Otto-Hahn-Str. 6, Dortmund, Germany D-44221 Further Advances in Germanium, Tin and Lead NMR Olga S. Volkova Institute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090 Radical Reaction Mechanisms of and at Organic Germanium, Tin and Lead Mikhail G. Voronkov A. E. Favorsky Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk, Russia 664033 Genesis and Evolution in the Chemistry of Organogermanium, Organotin and Organolead Compounds Similarities and Differences of Organic Compounds of Germanium, Tin and Lead Ilya Zharov University of Colorado, Department of Chemistry and Biochemistry, Boulder, CO, USA 80309-0215 Free and Complexed R3M+ Cations (M = Ge, Sn, Pb)

Phenols (2003) Volker Böhmer Johannes Gutenberg-Universität, Fachbereich Chemie und Pharmazie, Abteilung Lehramt Chemie, Duesbergweg 10–14, Mainz, Germany D-55099 Calixarenes C. Barclay Mount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8

Phenols as Antioxidants M. Berthelot University of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3, France F-44322 Hydrogen-Bonded Complexes of Phenols Luis Castedo Universidad de Santiago de Compostela, Departamento de Quí mica Orgánica y Unidad Asociada al C.S.I.C., Facultad de Quí mica, Santiago de Compostela, Spain 15782 Synthesis of Phenols M. J. Caulfield The University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne, Victoria, Australia 3010 Polymers based on phenols Victor Glezer Ministry of Health, National Public Health Laboratory, 69 Ben Zvi Rd., Tel Aviv, Israel Environmental Effects of Substituted Phenols Concepción González Universidad de Santiago de Compostela, Departamento de Quí mica Orgánica, Facultad de Ciencias, Lugo, Spain 27002 Synthesis of Phenols J. Graton University of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3, France F-44322 Hydrogen-Bonded Complexes of Phenols Poul Erik Hansen Roskilde University, Department of Life Sciences and Chemistry, Box 260, Roskilde, Denmark DK-4000

NMR and IR Spectroscopy of Phenols William M. Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN Photochemistry of Phenols Menahem Kaftory Technion—Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000 The Structural Chemistry of Phenols Eugene S. Kryachko University of Leuven, Department of Chemistry, Belgium B-3001 and Limburgs Universitaire Centrum, Departement SBG, Diepenbeek, Belgium B-3590 General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of Phenols Dietmar Kuck Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, Bielefeld, Germany D-33615 Mass Spectrometry and Gas-Phase Ion Chemistry of Phenols C. Laurence University of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3, France F-44322 Hydrogen-Bonded Complexes of Phenols Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry of Phenols and Related Arenols P. Neta National Institute of Standards and Technology, Gaithersburg, MD 20899, USA Radiation Chemistry of Phenols Transient Phenoxyl Radicals: Formation and Properties in Aqueous Solutions Minh Tho Nguyen University of Leuven, Department of Chemistry, Leuven, Belgium B-3001

General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of Phenols Ehud Pines Ben-Gurion University of the Negev, Chemistry Department, P.O.B. 653, Beer-Sheva, Israel 84105 UV-Visible Spectra and Photoacidity of Phenols, Naphthols and Pyrenols V. Prakash Reddy University of Missouri-Rolla, Department of Chemistry, Rolla, MO 65409, USA Electrophilic Reactions of Phenols G. G. Qiao The University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne, Victoria, Australia 3010 Polymers based on phenols L. Ross Mount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8 Phenols as Antioxidants Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry of Phenols and Related Arenols D. H. Solomon The University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne, Victoria, Australia 3010 Polymers based on phenols Jens Spanget-Larsen Roskilde University, Department of Life Sciences and Chemistry, Box 260, Roskilde, Denmark DK-4000 NMR and IR Spectroscopy of Phenols S. Steenken Max-Planck-Institut für Strahlenchemie, D-45413, Mülheim, Germany Radiation Chemistry of Phenols

Transient Phenoxyl Radicals: Formation and Properties in Aqueous Solutions G. K. Surya Prakash University of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry, Los Angeles, CA 90089-1661, USA Electrophilic Reactions of Phenols Luc G. Vanquickenborne University of Leuven, Department of Chemistry, Leuven, Belgium B-3001 General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of Phenols Melinda R. Vinqvist Mount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8 Phenols as Antioxidants Masahiko Yamaguchi Tohoku University, Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Aoba, Sendai, Japan 980-8578 Synthetic Uses of Phenols Shosuke Yamamura Keio University, Department of Chemistry, Faculty of Science and Technology, Hiyoshi, Yokohama, Japan 223-8522 Oxidation of Phenols Jacob Zabicky Institutes for Applied Research, Ben-Gurion University of the Negev, P. O. Box 653, Beer-Sheva, Israel 84105Analytical Aspects of Phenolic Compounds

Organolithium Compounds (2004) Manfred Braun Universität Düsseldorf, Institut für Organische Chemie und Makromolekulare Chemie, Düsseldorf, Germany D-40225 Lithium Carbenoids

Marvin Charton School of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA Effects of Structural Variation on Organolithium Compounds Fabrice Chemla Université Pierre et Marie Curie, Tour 44-45 2ème étage, Bte 183, Laboratoire de Chimie Organique, 4 Place Jussieu, Paris Cedex 05, France F-75252 Reactivity of Oxiranes with Organolithium Reagents Guido Christoph Organisch-Chemisches Institut der Westfälischen Wilhelms-Universität Münster, Corrensstr. 40, Münster, Germany D-48149 Asymmetric Deprotonation with Alkyllithium–(-)-Sparteine Jonathan Clayden University of Manchester, Department of Chemistry, Oxford Road, Manchester, UK M13 9PL Directed Metallation of Aromatic Compounds Iain Coldham University of Exeter, School of Chemistry, Stocker Road, Exeter, UK EX4 4QD α-Amino-Organolithium Compounds Chagit Denekamp Technion–Israel Institute of Technology, Department of Chemistry, Technion City, Haifa, Israel 32000 Gas Phase Chemistry of Organolithium Compounds Robert E. Gawley University of Miami, Department of Chemistry, Coral Gables, FL 33124, USA α-Amino-Organolithium Compounds G. Gopakumar University of Hyderabad, School of Chemistry, Gachibowli, Hyderabad, Andhra Pradesh, India 500 046 Theoretical Studies in Organolithium Chemistry

Harald Günther University of Siegen, OCII, Fachbereich 8, Siegen, Germany D-57068 Solid State NMR Spectroscopy in Organolithium Chemistry Dieter Hoppe Organisch-Chemisches Institut der Westfälischen Wilhelms-Universität Münster, Corrensstr. 40, Münster, Germany D-48149 Asymmetric Deprotonation with Alkyllithium–(-)-Sparteine Eluvathingal D. Jemmis University of Hyderabad, School of Chemistry, Gachibowli, Hyderabad, Andhra Pradesh, India 500 046 Theoretical Studies in Organolithium Chemistry Dan Johnels Umeå University, Department of Chemistry/Organic Chemistry, Umeå, Sweden SE-901 87 Solid State NMR Spectroscopy in Organolithium Chemistry W. Kiefer Universität Würzburg, Institut für Physikalische Chemie, Am Hubland, Würzburg, Germany D-97074 Vibrational Spectroscopy of Organolithium Compounds Frédéric Leroux Université Louis Pasteur (ECPM), Laboratoire de stéréochimie, 25 rue Becquerel, Strasbourg, France F-67087 The Preparation of Organolithium Reagents and Intermediates Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry of Organolithium Compounds Ilan Marek

Technion—Israel Institute of Technology, Department of Chemistry and Institute of Catalysis, Science and Technology, Technion City, Haifa, Israel 32000 The Preparation of Organolithium Reagents and Intermediates I. Pavel Universität Würzburg, Institut für Physikalische Chemie, Am Hubland, Würzburg, Germany D-97074 Vibrational Spectroscopy of Organolithium Compounds Daniel Schildbach Universität Würzburg, Institut für Anorganische Chemie, Am Hubland, Würzburg, Germany D-97074 Polylithium Organic Compounds: Syntheses and Selected Molecular Structures Manfred Schlosser Swiss Federal Institute of Technology, Institute of Molecular and Biological Chemistry, Lausanne, Switzerland CH-1015 The Preparation of Organolithium Reagents and Intermediates Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry of Organolithium Compounds D. Stalke Universität Würzburg, Institut für Anorganische Chemie, Am Hubland, Würzburg, Germany D-97074 Vibrational Spectroscopy of Organolithium Compounds Dietmar Stalke Am Hubland, Institut für Anorganische Chemie der Bayerischen Julius-Maximilians Universität Würzburg, Würzburg, Germany 97074 Lead Structures in Lithium Organic Chemistry Thomas Stey

Am Hubland, Institut für Anorganische Chemie der Bayerischen Julius-Maximilians Universität Würzburg, Würzburg, Germany 97074 Lead Structures in Lithium Organic Chemistry Carsten Strohmann Universität Würzburg, Institut für Anorganische Chemie, Am Hubland, Würzburg, Germany D-97074 Polylithium Organic Compounds: Syntheses and Selected Molecular Structures K. Tomioka Kyoto University, Graduate School of Pharmaceutical Sciences, Sakyo-ku, Yoshida, Kyoto, Japan 606–8501 Addition of Organolithium Reagents to Double Bonds Katsuhiko Tomooka Tokyo Institute of Technology, Department of Applied Chemistry, Meguro-ku, Tokyo, Japan 152-8552 Rearrangements of organolithium compounds Emmanuel Vrancken Université Pierre et Marie Curie, Tour 44-45 2ème étage, Bte 183, Laboratoire de Chimie Organique, 4 Place Jussieu, Paris Cedex 05, France F-75252 Reactivity of Oxiranes with Organolithium Reagents K. Yamada Kyoto University, Graduate School of Pharmaceutical Sciences, Sakyo-ku, Yoshida, Kyoto, Japan 606–8501 Addition of Organolithium Reagents to Double Bonds Hiroshi Yamataka Osaka University, Institute of Scientific and Industrial Research, Osaka, Ibaraki, Japan 567–0047 Addition of Organolithium Reagents to Double Bonds Miguel Yus Universidad de Alicante, Departamento de Química Orgánica, Facultad de Ciencias, Apdo. 99, Alicante, Spain 03080 Arene-Catalyzed Lithiation

Jacob Zabicky Ben-Gurion University of the Negev, Institutes for Applied Research, P. O. Box 653, Beer-Sheva, Israel 84105 Analytical Aspects of Organolithium Compounds Elinor Zohar Technion—Israel Institute of Technology, Department of Chemistry and Institute of Catalysis, Science and Technology, Technion City, Haifa, Israel 32000 The Preparation of Organolithium Reagents and Intermediates

Cyclobutanes (2005) José Luis M. Abboud Instituto de Química Física `Rocasolano', CSIC, C/Serrano, 119, Madrid, Spain E-28006 Acidity and Basicity of Cyclobutanes Ibon Alkorta Instituto de Química Médica, CSIC, C/Juan de la Cierva, 3, Madrid, Spain E-28006 Acidity and Basicity of Cyclobutanes A. Bashir-Hashemi ERC, Inc., at AFRL/PRS, 10 East Saturn Blvd., Edwards AFB, CA 93524, USA Chemistry of Cubane and Other Prismanes Nathan L. Bauld The University of Texas at Austin, Department of Chemistry and Biochemistry, Austin, TX 78731, USA Cation Radicals in the Synthesis and Reactions of Cyclobutanes Ulf Berg Lund University, Organic Chemistry 1, Department of Chemistry, P. O. Box 124, Lund, Sweden S-221 00 Stereochemical Aspects—Conformation and Configuration Holger Butenschön

Universität Hannover, Institut für Organische Chemie, Schneiderberg 1B, Hannover, Germany D-30167 Organometallic Derivatives Thomas Carell LMU München, Department of Chemistry, Butenandtstraße 5–13 Haus F, München, Germany D-81377 Cyclobutane Pyrimidine Dimers as UV-Induced DNA Lesions Barry K. Carpenter Cornell University, Department of Chemistry and Chemical Biology, Ithaca, NY 14853-1301, USA Bicyclo[2.1.0]pentanes and Bicyclo[2.2.0]hexanes Siu-Hin Chan The Chinese University of Hong Kong, Department of Chemistry, Institute of Chinese Medicine and Central Laboratory of Institute of Molecular Technology for Drug Discovery and Synthesis, Shatin, New Territories, Hong Kong SAR, Peoples’ Republic of China The Application of Cyclobutane Derivatives in Organic Synthesis Marvin Charton Pratt Institute, Chemistry Department, School of Liberal Arts and Sciences, Brooklyn, NY 11205, USA Structural Effects of the Cyclobutyl Group on Reactivity and Properties Xudong Chen Dartmouth College, Department of Chemistry, Hanover, NH 03755, USA Fluorinated Cyclobutanes and Their Derivatives Juan Z. Dávalos Instituto de Química Física `Rocasolano', CSIC, C/Serrano, 119, Madrid, Spain E-28006 Acidity and Basicity of Cyclobutanes Jacques Fernandes Dias Universidade Estadual do Rio de Janeiro, Departamento de Química e Ambiental, Faculdade de Tecnologia, Estrada Resende-Riachuelo s/n˚, Resende, Brazil RJ 27523-000 NMR Spectroscopy of Cyclobutanes M. Eckert-Maksić

Rudjer Bošković Institute, Laboratory for Physical-Organic Chemistry, Division of Organic Chemistry and Biochemistry, Quantum Organic Chemistry Group, Zagreb, Croatia Antiaromaticity and Aromaticity in Carbocyclic Four-Membered Rings Marcus G. Friedel LMU München, Department of Chemistry, Butenandtstraße 5–13 Haus F, München, Germany D-81377 Cyclobutane Pyrimidine Dimers as UV-Induced DNA Lesions Nan-Yan Fu The Chinese University of Hong Kong, Department of Chemistry, Institute of Chinese Medicine and Central Laboratory of Institute of Molecular Technology for Drug Discovery and Synthesis, Shatin, New Territories, Hong Kong SAR, Peoples’ Republic of China The Application of Cyclobutane Derivatives in Organic Synthesis Johannes Gierlich LMU München, Department of Chemistry, Butenandtstraße 5–13 Haus F, München, Germany D-81377 Cyclobutane Pyrimidine Dimers as UV-Induced DNA Lesions Hiroyuki Higuchi Toyama University, Department of Chemistry, Faculty of Science, 3190 Gofuku, Toyama, Toyama, Japan 930-8555 Chemistry of Cubane and Other Prismanes Henning Hopf Technical University of Braunschweig, Institute of Organic Chemistry, Hagenring 30, Braunschweig, Germany D-38106 Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other Oligocyclobutanoids William M. Horspool The University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN Photochemistry of Cyclobutanes: Synthesis and Reactivity

Richard P. Johnson University of New Hampshire, Department of Chemistry, Durham, NH 03824, USA Highly Unsaturated Cyclobutane Derivatives Dietmar Kuck Universität Bielefeld, Fakultät für Chemie, Universitätsstraße 25, Bielefeld, Germany D-33501 Mass Spectrometry and Gas-Phase Ion Chemistry of Cyclobutanes E. Lee-Ruff York University, Department of Chemistry, Toronto, Ontario, Canada M3J 1P3 Synthesis of Cyclobutanes David M. Lemal Dartmouth College, Department of Chemistry, Hanover, NH 03755, USA Fluorinated Cyclobutanes and Their Derivatives Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other Oligocyclobutanoids Thermochemistry of Cyclobutane and Its Derivatives Z. B. Maksić Rudjer Bošković Institute, Laboratory for Physical-Organic Chemistry, Division of Organic Chemistry and Biochemistry, Quantum Organic Chemistry Group, Zagreb, Croatia Antiaromaticity and Aromaticity in Carbocyclic Four-Membered Rings Arunkumar Natarajan Tulane University, Department of Chemistry, New Orleans, LA 70118, USA Solvent-Free Photosynthesis of Cyclobutanes: Photodimerization of Crystalline Olefins H. Mark Perks University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other Oligocyclobutanoids Esther Quintanilla Instituto de Química Física `Rocasolano', CSIC, C/Serrano, 119, Madrid, Spain E-28006

Acidity and Basicity of Cyclobutanes V. Ramamurthy Tulane University, Department of Chemistry, New Orleans, LA 70118, USA Solvent-Free Photosynthesis of Cyclobutanes: Photodimerization of Crystalline Olefins Peter Rudolf Seidl Universidade Federal do Rio de Janeiro, Centro de Tecnologia Bloco E, Ilha do Fundão, Departamento de Processos Orgânicos, Escola de Química, Rio de Janeiro, RJ, Brazil 21949-900 NMR Spectroscopy of Cyclobutanes Hans-Ullrich Siehl Abteilung Organische Chemie I der Universität Ulm, Albert Einstein Allee 11, Ulm, Germany D-89069 Cyclobutyl, Cyclobutyl-Substituted and Related Carbocations Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry of Cyclobutane and Its Derivatives Amnon Stanger Technion—Israel Institute of Technology, Department of Chemistry, The Lise Meitner-Minerva Center for Computational Quantum Chemistry, The Institute of Catalysis, Science and Technology, Haifa, Israel 32000 Cyclobutarenes J. M. Tanko Virginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061, USA Rearrangements of Cyclobutanes Kenneth B. Wiberg Yale University, Department of Chemistry, New Haven, CT 06520-8107, USA Cyclobutane—Physical Properties and Theoretical Studies

Organolithium Compounds (2006) Per Ahlberg Göteborg University, Department of Chemistry, Göteborg, Sweden SE-41296 Chiral Lithium Amides in Asymmetric Synthesis Mohamed Amedjkouh Göteborg University, Department of Chemistry, Göteborg, Sweden SE-41296 Chiral Lithium Amides in Asymmetric Synthesis Ivan Aprahamian The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 The Lithium Metal Reduction of π-Conjugated Hydrocarbons and Fullerenes Francisco J. Fañanás Universidad de Oviedo, Instituto Universitario de Química Organometálica ``Enrique Moles'', Unidad Asociada al CSIC, C/Julián Clavería, 8, Oviedo, Spain E-33006 Intramolecular Carbolithiation Reactions Gideon Fraenkel The Ohio State University, Department of Chemistry, 100 W. 18th Avenue, Columbus, OH 43210, USA Dynamics of the Reorganization Behavior of Organolithium Compounds Johan Granander Göteborg University, Department of Chemistry, Kemivägen 10, Göteborg, Sweden SE-412 96 Structure and Dynamics of Chiral Lithium Amides Göran Hilmersson Göteborg University, Department of Chemistry, Kemivägen 10, Göteborg, Sweden SE-412 96 Structure and Dynamics of Chiral Lithium Amides Jacques Maddaluno

Université de Rouen, Laboratoire des Fonctions Azotées & Oxygénées Complexes de l'IRCOF, UMR 6014 CNRS, Mont St Aignan Cedex, France F-76821 Aspects of the Synthesis, Structure and Reactivity of Lithium Enolates Carmen Najera Universidad de Alicante, Departamento de Química Orgánica, Facultad de Ciencias, and Instituto de Síntesis Orgánica (ISO), Apdo. 99, Alicante, Spain E-03080 The Chemistry of Acyllithium Derivatives Hiroyuki Nakahira Sumitomo Pharmaceuticals, Chemistry Research Laboratories, Research Division, Osaka, Japan 554-0022 Chemistry of Ketone Dilithio Dianions Daniel Pettersen Göteborg University, Department of Chemistry, Göteborg, Sweden SE-41296 Chiral Lithium Amides in Asymmetric Synthesis Mordecai Rabinovitz The Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904 The Lithium Metal Reduction of π-Conjugated Hydrocarbons and Fullerenes Ilhyong Ryu Osaka Prefecture University, Department of Chemistry, Graduate School of Science, Sakai, Osaka, Japan 599–8531 Chemistry of Ketone Dilithio Dianions Roberto Sanz Universidad de Burgos, Departamento de Química, Facultad de Ciencias, Plaza Missael Bañuelos s/n, Burgos, Spain E-09001 Intramolecular Carbolithiation Reactions Norma Sbarbati Nudelman Universidad de Buenos Aires, Depto. Química Orgánica, Facultad de Ciencias Exactas y Naturales, Pab. II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina Organolithiums as Useful Synthetic Intermediates for Tandem Reactions Jean-Yves Valnot

Université de Rouen, Laboratoire des Fonctions Azotées & Oxygénées Complexes de l'IRCOF, UMR 6014 CNRS, Mont St Aignan Cedex, France F-76821 Aspects of the Synthesis, Structure and Reactivity of Lithium Enolates Alvaro J. Vázquez Universidad de Buenos Aires, Depto. Química Orgánica, Facultad de Ciencias Exactas y Naturales, Pab. II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina Organolithiums as Useful Synthetic Intermediates for Tandem Reactions Raquel G. de Waisbaum Universidad de Buenos Aires, Depto. Química Orgánica, Facultad de Ciencias Exactas y Naturales, Pab. II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina Organolithiums as Useful Synthetic Intermediates for Tandem Reactions Miguel Yus Universidad de Alicante, Departamento de Química Orgánica, Facultad de Ciencias, and Instituto de Síntesis Orgánica (ISO), Apdo. 99, Alicante, Spain E-03080 The Chemistry of Acyllithium Derivatives

Peroxides (2006) Waldemar Adam University of Würzburg, Institute of Organic Chemistry, am Hubland, Würzburg, Germany D-97094and University of Puerto Rico, Department of Chemistry, Rio Piedras, Puerto Rico 00931, USA Contemporary Dioxirane Chemistry: Epoxidations, Heteroatom Oxidations and CH Insertions Contemporary Trends in Dioxetane Chemistry Wataru Ando University of Tsukuba, Department of Chemistry, Tennodai, Tsukuba, Ibaraki, Japan 305–8577 Silicon and Germanium Peroxides

Wilhelm J. Baader Universidade de São Paulo-Av. Prof. Lineu Prestes, Instituto de Química, 748 Bl., 12 S CEP, São Paulo—SP, Brazil 05508-900 Chemiluminescence of Organic Peroxides Robert D. Bach University of Delaware, Department of Chemistry and Biochemistry, Newark, DE 19716, USA General and Theoretical Aspects of the Peroxide Group Mario D. Bachi The Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100 Synthesis of Cyclic Peroxides Erick L. Bastos Universidade de São Paulo-Av. Prof. Lineu Prestes, Instituto de Química, 748 Bl., 12 S CEP, São Paulo—SP, Brazil 05508-900 Chemiluminescence of Organic Peroxides Albrecht Berkessel University of Cologne, Department of Organic Chemistry, Greinstr. 4, Koln, Germany D-50939 Synthetic Uses of Peroxides Olga Bortolini Università della Calabria, Dipartimento di Chimica, Via Bucci, cubo 12C, Rende (CS), Italy I-87036 Transition Metal Peroxides. Synthesis and Role in Oxidation Reactions Jean Cadet LCIB-UMR-E n˚3 CEA-UJF, Laboratoire `Lésions des Acides Nucléiques', Département de Recherche Fondamentale sur la Matière Condensée, Grenoble Cedex 9, CEA/Grenoble, France F-38054 Peroxides in Biological Systems

Giovanni Cerioni Università di Cagliari, Dipartimento Farmaco Chimico Tecnologico, Via Ospedale 72, Cagliari, Italy I-09124 17O NMR Spectroscopy of Organic Compounds Containing the –O–O–group James Chadwick University of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UK L69 7ZD Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour Endoperoxides Valeria Conte Università di Roma ``Tor Vergata'', Dipartimento di Scienze e Tecnologie Chimiche, via della Ricerca Scientifica, Roma, Italy I-00133 Transition Metal Peroxides. Synthesis and Role in Oxidation Reactions Paolo Di Mascio Universidade de São Paulo, Ar. Prof. Lineu Prestes, Departamento de Bioquímica, Instituto de Química, 748 CP 26077, São Paulo, SP, Brazil CEP 05513-970 Peroxides in Biological Systems Jens Hartung Technische Universität Kaiserslautern, Fachbereich Chemie, Organische Chemie, Erwin-Schrödinger-Straße, Kaiserslautern, Germany D-67663 The Structural Chemistry of Acyclic Organic Peroxides Vidyadhar Jadhav Korea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis, Department of Chemistry, Taejon, Korea 305-701 Sulfur and Phosphorus Peroxides Sung Soo Kim Inha University, Department of Chemistry, Incheon, South Korea 402-751 Polar Effects in Decomposition of Peroxidic Compounds and Related Reactions Yong Hae Kim

Korea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis, Department of Chemistry, Taejon, Korea 305-701 Sulfur and Phosphorus Peroxides Edward E. Korshin The Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100 Synthesis of Cyclic Peroxides Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry of Peroxides Francesca Mocci Università di Cagliari, Cittadella Universitaria di Monserrato, Dipartimento di Scienze Chimiche, SS 554 Bivio per Sestu, Monserrato, (CA), Italy I-09024 17O NMR Spectroscopy of Organic Compounds Containing the –O–O–group Paul M. O'Neill University of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UK L69 7ZD Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour Endoperoxides Michael Orfanopoulos University of Crete, Department of Chemistry, Iraklion, Greece G-71409 Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene Reaction Min Young Park Korea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis, Department of Chemistry, Taejon, Korea 305-701 Sulfur and Phosphorus Peroxides Sarah L. Rawe University of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UK L69 7ZD

Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour Endoperoxides Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry of Peroxides C. V. Stevani Universidade de São Paulo-Av. Prof. Lineu Prestes, Instituto de Química, 748 Bl., 12 S CEP, São Paulo—SP, Brazil 05508-900 Chemiluminescence of Organic Peroxides Manolis Stratakis University of Crete, Department of Chemistry, Iraklion, Greece G-71409 Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene Reaction Ingrid Svoboda Technische Universität Darmstadt, Fachgebiet Strukturforschung, FB 11, Material-und Geowissenschaften, Petersenstr. 23, Darmstadt, Germany D-64287 The Structural Chemistry of Acyclic Organic Peroxides Alexei V. Trofimov Russian Academy of Sciences, Institute of Biochemical Physics, ul. Kosygina 4, Moscow, Russian Federation 119991 and University of Würzburg, Institute of Organic Chemistry, am Hubland, Würzburg, Germany D-97094 Contemporary Trends in Dioxetane Chemistry Nadine Vogl University of Cologne, Department of Organic Chemistry, Greinstr. 4 Germany D-50939 Koln Synthetic Uses of Peroxides Georgios C. Vougioukalakis University of Crete, Department of Chemistry, Iraklion, Greece G-71409

Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene Reaction Jacob Zabicky Ben-Gurion University of the Negev, Institutes for Applied Research, Department of Chemical Engineering, Beer-Sheva, Israel 84105 Analytical and Safety Aspects of Organic Peroxides and Related Functional Groups Cong-Gui Zhao University of Texas at San Antonio, Department of Chemistry, San Antonio, TX 78249, USA Contemporary Dioxirane Chemistry: Epoxidations, Heteroatom Oxidations and CH Insertions

Anilines (2007) Daniella Vasconcellos Augusti Octávio Magalhães Institute, Ezequiel Diaz Foundation—FUNED, Belo Horizonte, MG, Brazil 30510-010 Mass Spectrometry and Gas-Phase Chemistry of Anilines Rodinei Augusti Federal University of Minas Gerais—UFMG, Department of Chemistry, Belo Horizonte, MG, Brazil 31270-901 Mass Spectrometry and Gas-Phase Chemistry of Anilines Fabiola Barrios-Landeros Yale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA Synthesis of Anilines Marcos N. Eberlin State University of Campinas, ThoMSon Mass Spectrometry Laboratory, Institute of Chemistry, Campinas, SP, Brazil 13084 971 Mass Spectrometry and Gas-Phase Chemistry of Anilines Luciano Forlani

University of Bologna, Dipartimento di Chimica Organica `A. Mangini', Viale Risorgimento 4, Bologna, Italy 40136 Hydrogen Bonds of Anilines Ryszard Gawinecki Faculty of Chemical Technology and Engineering, University of Technology and Life Sciences, Seminaryjna 3, Bydgoszcz, PL, Poland 85 326 NMR Spectra of Anilines John F. Hartwig Yale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA Synthesis of Anilines Jan S. Jaworski Warsaw University, Faculty of Chemistry, Warszawa, Poland 02-093 Electrochemistry of Anilines Marek K. Kalinowski Warsaw University, Faculty of Chemistry, Warszawa, Poland 02-093 Electrochemistry of Anilines Alla V. Koblik ChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435 Rearrangements of Anilines and Their Derivatives Erkki Kolehmainen University of Jyväskylä, Department of Chemistry, P.O. Box 35, Finland FIN-40014 NMR Spectra of Anilines Ikchoon Lee Inha University, Department of Chemistry, Inchon, Korea 402-751 Anilines as nucleophiles Joel F. Liebman University of Maryland Balimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA

Thermochemistry of Anilines Sergei M. Lukyanov ChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435 Rearrangements of Anilines and Their Derivatives Yizhak Marcus The Hebrew University of Jerusalem, Department of Inorganic and Analytical Chemistry, Jerusalem, Israel 91904 Substituted Anilines as Solvatochromic Probes Minh Tho Nguyen University of Leuven, Department of Chemistry and Institute for Nanoscale Physics and Chemistry, Celestijnenlaan 200F, Leuven, Belgium B-3001 General and Theoretical Aspects of Anilines Borys Ośmiałowski Faculty of Chemical Technology and Engineering, University of Technology and Life Sciences, Seminaryjna 3, Bydgoszcz, PL, Poland 85 326 NMR Spectra of Anilines Valery A. Ozeryanskii Rostov State University, Department of Organic Chemistry, Zorge str., 7, Rostov-on-Don, Russian Federation 344090 Proton Sponges Alexander F. Pozharskii Rostov State University, Department of Organic Chemistry, Zorge str., 7, Rostov-on-Don, Russian Federation 344090 Proton Sponges Shashank Shekhar Yale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA Synthesis of Anilines Qilong Shen

Yale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA Synthesis of Anilines Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry of Anilines Dae Dong Sung Dong-A University, Department of Chemistry, Busan, Korea 604-714 Anilines as nucleophiles Anthony S. Travis The Hebrew University of Jerusalem, Sidney M. Edelstein Center for the History and Philosophy of Science, Technology and Medicine, Edmond J. Safra Campus, Givat Ram, Jerusalem, Israel 91904 Anilines: Historical Background Manufacture and Uses of the Anilines: A Vast Array of Processes and Products Toxicological and Environmental Aspects of Anilines Grażyna Maria Wójcik Wrocław University of Technology, Institute of Physical & Theoretical Chemistry, Wyb. Wyspiańskiego 27, Wrocław, Poland 50-370 Structural Chemistry of Anilines Jye-Shane Yang National Taiwan University, Department of Chemistry, Taipei, Taiwan (ROC) 10617 The Spectroscopy, Photophysics and Photochemistry of Anilines Jacob Zabicky Ben-Gurion University of the Negev, Department of Chemical Engineering, P.O. Box 653, Beer-Sheva, Israel 84105

Analytical Aspects of Aromatic Amines

Organozinc Compounds (2007) Varinder K. Aggarwal University of Bristol, School of Chemistry, Cantock's Close, Bristol, United Kingdom BS8 1TS Rearrangements of Organozinc Compounds Jaap Boersma Utrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, The Netherlands 3584 Structural Organozinc Chemistry Olivier Buriez Université Paris XII, C.N.R.S. UMR 7582, Laboratoire d'Electrochimie Catalyse et Synthése Organique, 2-8 rue H. Dunant, Thiais, France F-94320 Electrochemical Generation and Reaction of Zinc Reagents Donald J. Burton University of Iowa, Department of Chemistry, Iowa City, IA 52242, USA Fluorinated Organozinc Reagents André B. Charette Université de Montréal, Department of Chemistry, P.O. Box 6128, Station Downtown, Montréal, Québec, Canada H3C 3J7 Cyclopropanation Mediated by Zinc Organometallics Timothy Clark University of Erlangen-Nürnberg, Computer Chemistry Center, Nägelsbachstr. 25, Erlangen, Germany D-91052 The Reaction Mechanisms of Zinc Enzymes Athanassios G. Coutsolelos University of Crete, Chemistry Department, Laboratory of Bioinorganic Chemistry, PO Box 2208, Heraklion, Crete, Greece GR-71003

67Zn NMR, a Tool for Coordination Chemistry Problems Charles R. Davis Sigma-Aldrich, 6000 N. Teutonia Avenue, Milwaukee, WI 53209, USA Fluorinated Organozinc Reagents Rudi van Eldik University of Erlangen-Nürnberg, Institute for Inorganic Chemistry, Egerlandstr. 1, Erlangen, Germany D-91058 The Reaction Mechanisms of Zinc Enzymes Liu-Zhu Gong Ludwig-Maximilians-Universität München, Department of Chemistry, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organozinc Compounds Corinne Gosmini Université Paris XII, C.N.R.S. UMR 7582, Laboratoire d'Electrochimie Catalyse et Synthése Organique, 2-8 rue H. Dunant, Thiais, France F-94320 Electrochemical Generation and Reaction of Zinc Reagents Albert Guijarro Universidad de Alicante, Departamento de Química Orgánica, Instituto de Síntesis Orgánica (ISO), Ap. 99, Alicante, Spain E-03080 Dynamic Behavior of Organozinc Compounds Toshiro Harada Kyoto Institute of Technology, Department of Chemistry and Materials Technology, Matsugasaki, Sakyo-ku, Kyoto, Japan 606-8585 The Chemistry of Organozincate Compounds Qian Hu Purdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN 47907-2084, USA Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and Related Organometals Zhihong Huang

Purdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN 47907-2084, USA Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and Related Organometals Johann T. B. H. Jastrzebski Utrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, The Netherlands 3584 Structural Organozinc Chemistry Tsuneomi Kawasaki Tokyo University of Science, Department of Applied Chemistry, Faculty of Science, Kagurazaka, Shinjuku-ku, Tokyo, Japan 162-8601 Enantioselective Addition of Organozinc Compounds Florian F. Kneisel Ludwig-Maximilians-Universität München, Department of Chemistry, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organozinc Compounds Paul Knochel Ludwig-Maximilians-Universität München, Department of Chemistry, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organozinc Compounds Gerard van Koten Utrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, The Netherlands 3584Structural Organozinc Chemistry Helena Leuser Ludwig-Maximilians-Universität München, Department of Chemistry, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organozinc Compounds Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, , USA MD 21250, USA Thermochemistry of Organozinc Compounds

Marco Lombardo University of Bologna, Department of Chemistry ``G. Ciamician'', via Selmi 2, Bologna, Italy I-40126 The Chemistry of Zinc Enolates Edwige Lorthiois Novartis Pharma AG, Novartis Institutes for Biomedical Research, Protease Platform WKL-122-3-27, Klybeckstrasse 144, Basel, Switzerland CH-4002 Carbozincation of Alkenes and Alkynes James A. Marshall University of Virginia, Department of Chemistry, PO Box 400319, Charlottesville, VA 22904, USA Synthesis and Reactions of Allenylzinc Reagents Seijiro Matsubara Kyoto University, Department of Material Chemistry, Graduate School of Engineering, Kyoudai-katsura, Nishikyo, Kyoto, Japan 606-8501 1,1-Bismetallated Species Christophe Meyer associé au CNRS, ESPCI, Laboratoire de Chimie Organique, 10 rue Vauquelin, Paris Cedex 05, France F-75231 Carbozincation of Alkenes and Alkynes Ei-Ichi Negishi Purdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN 47907-2084, USA Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and Related Organometals Sergiu P. Palii University of Florida, Department of Chemistry, P.O. Box 117200, Gainesville, FL 32611-7200, USA Mass Spectrometry of Organozinc Compounds Jacques Périchon

Université Paris XII, C.N.R.S. UMR 7582, Laboratoire d'Electrochimie Catalyse et Synthése Organique, 2-8 rue H. Dunant, Thiais, France F-94320 Electrochemical Generation and Reaction of Zinc Reagents Sylvie Perrone Ludwig-Maximilians-Universität München, Department of Chemistry, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organozinc Compounds Itaru Sato Kwansei Gakuin University, Department of Chemistry, School of Science and Technology, Sanda, Hyogo, Japan 669–1337 Enantioselective Addition of Organozinc Compounds Gudrun Schürer University of Erlangen-Nürnberg, Computer Chemistry Center, Nägelsbachstr. 25, Erlangen, Germany D-91052 The Reaction Mechanisms of Zinc Enzymes Mathias O. Senge Trinity College Dublin, School of Chemistry, Dublin 2, Ireland Photochemical Transformations Involving Zinc Porphyrins and Phthalocyanines Natalia N. Sergeeva Trinity College Dublin, School of Chemistry, Dublin 2, Ireland Photochemical Transformations Involving Zinc Porphyrins and Phthalocyanines Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemistry of Organozinc Compounds Kenso Soai

Tokyo University of Science, Department of Applied Chemistry, Faculty of Science, Kagurazaka, Shinjuku-ku, Tokyo, Japan 162-8601 Enantioselective Addition of Organozinc Compounds Knut Sommer University of Bristol, School of Chemistry, Cantock's Close, Bristol, United Kingdom BS8 1TS Rearrangements of Organozinc Compounds Georgios A. Spyroulias University of Patras, Department of Pharmacy, Panepistimioupoli—Rion, Patras, Greece GR-26504 67Zn NMR, a Tool for Coordination Chemistry Problems Claudio Trombini University of Bologna, Department of Chemistry ``G. Ciamician'', via Selmi 2, Bologna, Italy I-40126 The Chemistry of Zinc Enolates Guangwei Wang Purdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN 47907-2084, USA Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and Related Organometals Ning Yin Purdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN 47907-2084, USA Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and Related Organometals Dmitri V. Zagorevskii Rensselaer Polytechnic Institute, Department of Chemistry and Chemical Biology, 209C Cogswell Laboratories, 110 8th Str., Troy, NY 12180, USA Mass Spectrometry of Organozinc Compounds

Hydroxylamines, Oximes and Hydroxamic Acids (2008) Edgars Abele Latvian Institute of Organic Synthesis, Riga, Latvia LV1006 Synthesis of Heterocycles from Oximes Yacov Ashani The Weizmann Institute of Science, Department of Neurobiology, Rehovot, Israel 76100 Hydroxylamines and Oximes: Biological Properties and Potential Uses as Therapeutic Agents Yaniv Barda Weizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100 Natural and Biomimetic Hydroxamic Acid Based Siderophores Harald Brand LMU Munich, Butenandt-Str. 5-13, München, Germany 81377 Nitrosomethanides and their Acids: Synthesis, Structure and Bonding Erwin Buncel Queen's University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6 Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in Dephosphorylation Marvin Charton Pratt Institute, Chemistry Department, School of Liberal Arts and Sciences, Brooklyn, NY 11205, USA Structural Effects on Reactivity and Properties of Oximes and Hydroxamic Acids Ender Erdik Ankara University Science Faculty, Department of Chemistry, Beşevler, Ankara, Turkey 06100 Electrophilic C-Amination with O-Substituted Hydroxylamines, Oximes and O-Substituted Oximes Clifford E. Felder

Weizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100 Natural and Biomimetic Hydroxamic Acid Based Siderophores Jacques Fernandes Dias Universidade do Estado do Rio de Janeiro, Departamento de Química e Ambiental, Faculdade de Tecnologia, Rodovia Presidente Dutra km 298—Pólo Industrial, Resende, Brazil RJ 27537-000 NMR Spectra of Hydroxylamines, Oximes and Hydroxamic Acids Carlo Galli Università `La Sapienza' and IMC-CNR Sezione Meccanismi di Reazione, Dipartimento di Chimica, Roma, Italy 00185 Nitroxyl Radicals Giampaolo Giacomelli Università degli Studi di Sassari, Dipartimento di Chimica, via Vienna 2, Italy 07100-Sassari Synthesis of Oximes and Hydroxamic Acids Stephen A. Glover University of New England, Division of Chemistry School of Science and Technology, Armidale, NSW , Australia 2351 N-Heteroatom-Substituted Hydroxamic Esters Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA The Organic Thermochemistry of Hydroxylamines, Oximes, Hydroxamic Acids and their Derivatives Use of Oximes, Hydroxamic Acids and Related Species as Reagents in Inorganic Analytical Chemistry Edmunds Lukevics Latvian Institute of Organic Synthesis, Riga, Latvia LV1006

Synthesis of Heterocycles from Oximes Artem Melman Clarkson University, Department of Chemistry and Biomolecular Science, Potsdam, NY 13699, USA Synthesis of Hydroxylamines Jane S. Murray Cleveland State University, Department of Chemistry, Cleveland, OH 44115, USA Some Intrinsic Features of Hydroxylamines, Oximes and Hydroxamic Acids: Integration of Theory and Experiment Structural Analysis of Hydroxylamines, Oximes and Hydroxamic Acids: Trends and Patterns Osamu Onomura Nagasaki University, Department of Molecular Medicinal Sciences, Graduate School of Biomedical Sciences, 1-14, Bunkyo-machi, Nagasaki, Japan 852-8521 Electrochemistry of Hydroxylamines, Oximes and Hydroxamic Acids M. Manuela A. Pereira Universidade Nova de Lisboa, REQUIMTE/CQFB, Departamento de Química, Faculdade de Ciências e Tecnologia, Campus da Caparica, Caparica, Portugal 2829-516 Rearrangements of Hydroxylamines, Oximes and Hydroxamic Acids Peter Politzer University of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA Some Intrinsic Features of Hydroxylamines, Oximes and Hydroxamic Acids: Integration of Theory and Experiment Structural Analysis of Hydroxylamines, Oximes and Hydroxamic Acids: Trends and Patterns Maja Ponikvar Jožef Stefan Institute, Department of Inorganic Chemistry and Technology, Jamova 39, Ljubljana, Slovenia SI-1000

Use of Oximes, Hydroxamic Acids and Related Species as Reagents in Inorganic Analytical Chemistry Andrea Porcheddu Università degli Studi di Sassari, Dipartimento di Chimica, via Vienna 2, Sassari, Italy 07100- Synthesis of Oximes and Hydroxamic Acids Peter Rudolf Seidl Universidade Federal do Rio de Janeiro, Centro de Tecnologia, Departamento de Processos Orgânicos, Escola de Química, Bloco E, Ilha do Fundão, Rio de Janeiro, Brazil RJ 21949-900 NMR Spectra of Hydroxylamines, Oximes and Hydroxamic Acids Pedro Paulo Santos Universidade Técnica de Lisboa, Centro de Química Estrutural, Instituto Superior Técnico, Av. Rovisco Pais, Lisboa, Portugal 1049-001 Rearrangements of Hydroxylamines, Oximes and Hydroxamic Acids Axel Schulz Universität Rostock, Institut für Chemie, Abteilung Anorganische Chemie, Albert-Einstein-Straße 3a, Rostock, Germany 18059and Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Str. 29a, Rostock, Germany 18059 Nitrosomethanides and their Acids: Synthesis, Structure and Bonding Abraham Shanzer Weizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100 Natural and Biomimetic Hydroxamic Acid Based Siderophores Israel Silman The Weizmann Institute of Science, Department of Neurobiology, Rehovot, Israel 76100 Hydroxylamines and Oximes: Biological Properties and Potential Uses as Therapeutic Agents Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA

The Organic Thermochemistry of Hydroxylamines, Oximes, Hydroxamic Acids and their Derivatives François Terrier Université de Versailles, Institut Lavoisier, 45 Avenue des Etats-Unis 78035, Versailles Cedex, France UMR 8180 Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in Dephosphorylation Ik Hwan Um Ewha Womans University, Division of Nano Sciences and Department of Chemistry, Seoul, Korea 120-750 Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in Dephosphorylation Alexander Villinger Universität Rostock, Institut für Chemie, Abteilung Anorganische Chemie, Albert-Einstein-Straße 3a, Rostock, Germany 18059 Nitrosomethanides and their Acids: Synthesis, Structure and Bonding

Organomagnesium Compounds (2008) Jaap Boersma Faculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH, The Netherlands 3584 Structural Organomagnesium Chemistry Katja Brade Ludwig-Maximilians-Universität München, Department Chemie und Biochemie, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organomagnesium Compounds: Synthesis and Reactivity Gérard Cahiez UMR 8123 CNRS-ESCOM-UCP, Laboratoire de Synthèse Organique Sélective et de Chimie Organométallique (SOSCO), 5 Mail Gay Lussac, Cergy-Pontoise, Neuvilles/Oise, France F-95092 Iron-Catalyzed Reactions of Grignard Reagents Christophe Duplais

UMR 8123 CNRS-ESCOM-UCP, Laboratoire de Synthèse Organique Sélective et de Chimie Organométallique (SOSCO), 5 Mail Gay Lussac, Cergy-Pontoise, Neuvilles/Oise, France F-95092 Iron-Catalyzed Reactions of Grignard Reagents Ben L. Feringa University of Groningen, Stratingh Institute for Chemistry, Nijenborgh 4, Groningen, AG, The Netherlands 9747 Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using Grignard Reagents Andrey Gavryushin Ludwig-Maximilians-Universität München, Department Chemie und Biochemie, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organomagnesium Compounds: Synthesis and Reactivity Claude Grison UMR CNRS-Université de Montpellier 2 5032, ENSCM, 8 rue de l'Ecole Normale, Montpellier, France F-34296Preparation and Reactivity of Magnesium Enolates Peter J. Heard Birkbeck University of London, School of Biological and Chemical Sciences, Malet Street, London, UK WC1E 7HX NMR of Organomagnesium Compounds Kenneth W. Henderson University of Notre Dame, Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, Notre Dame, IN 46556, USA Organomagnesium-Group 15- and Organomagnesium-Group 16-Bonded Complexes Torkil Holm Technical University of Denmark, Department of Chemistry, Building 201, Lyngby, Denmark DK-2800 The Thermochemistry of Organomagnesium Compounds Katherine L. Hull University of Notre Dame, Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, Notre Dame, IN 46556, USA Organomagnesium-Group 15- and Organomagnesium-Group 16-Bonded Complexes Kenichiro Itami

Nagoya University, Department of Chemistry and Research Center for Materials Science, Chikusa-ku, Nagoya, Japan 464-8602 Carbomagnesiation Reactions Johann T. B. H. Jastrzebski Faculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH, The Netherlands 3584 Structural Organomagnesium Chemistry Jan S. Jaworski University of Warsaw, Faculty of Chemistry, Warszawa, Poland 02-093 Electrochemistry of Organomagnesium Compounds Paul Knochel Ludwig-Maximilians-Universität München, Department Chemie und Biochemie, Butenandtstr. 5-13, München, Germany D-81377 Functionalized Organomagnesium Compounds: Synthesis and Reactivity Gerard Van Koten Faculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH, The Netherlands 3584 Structural Organomagnesium Chemistry Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA The Thermochemistry of Organomagnesium Compounds Fernando López Universidad de Santiago de Compostela, Departamento de Química Orgánica, Facultad de Química, Avda. de las ciencias, s/n, Santiago de Compostela, Spain 15782 Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using Grignard Reagents Adriaan J. Minnaard University of Groningen, Stratingh Institute for Chemistry, Nijenborgh 4, Groningen, AG, The Netherlands 9747

Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using Grignard Reagents Richard A. J. O'Hair The University of Melbourne, School of Chemistry, Bio21 Molecular Science and Biotechnology Institute, ARC Centre of Excellence in Free Radical Chemistry and Biotechnology, Victoria, Australia 3010 Formation, Chemistry and Structure of Organomagnesium Species in Solvent-Free Environments Koichiro Oshima Kyoto University, Kyoto-daigaku Katsura, Department of Material Chemistry, Graduate School of Engineering, Kyoto, Nishikyo, Japan 615-8510 The Chemistry of Organomagnesium Ate Complexes Tsuyoshi Satoh Tokyo University of Science, Department of Chemistry, Faculty of Science, Ichigaya-funagawara-machi 12, Tokyo, Shinjuku-ku, Japan 162-0826 The Chemistry of Magnesium Carbenoids Mathias O. Senge Trinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland Photochemical Transformations Involving Magnesium Porphyrins and Phthalocyanines Natalia N. Sergeeva Trinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland Photochemical Transformations Involving Magnesium Porphyrins and Phthalocyanines Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA The Thermochemistry of Organomagnesium Compounds James Weston Friedrich-Schiller-Universität, Institut für Organische Chemie und Makromolekulare Chemie, Humboldtstraße 10, Jena, Germany D-07743 Biochemistry of Magnesium

Shinichi Yamabe Nara University of Education, Department of Chemistry, Takabatake-cho, Nara, Japan 630-8528 Theoretical Studies of the Addition of RMgX to Carbonyl Compounds Shoko Yamazaki Nara University of Education, Department of Chemistry, Takabatake-cho, Nara, Japan 630-8528 Theoretical Studies of the Addition of RMgX to Carbonyl Compounds Hideki Yorimitsu Kyoto University, Kyoto-daigaku Katsura, Department of Material Chemistry, Graduate School of Engineering, Kyoto, Nishikyo, Japan 615-8510 The Chemistry of Organomagnesium Ate Complexes Jun-Ichi Yoshida Kyoto University, Graduate School of Engineering, Department of Synthetic Chemistry and Biological Chemistry, Nishikyo-ku, Kyoto, Japan 615-8510 Carbomagnesiation Reactions Jacob Zabicky Ben-Gurion University of the Negev, Department of Chemical Engineering, P. O. Box 653, Beer-Sheva, Israel 84105 Analytical Aspects of Organomagnesium Compounds

Metal Enolates (2009) Juan Andrés Universitat Jaume I, Departament de Química Física y Analítica, Castelló, Spain 12071 General and Theoretical Aspects of the Metal Enolates Ksenija Babić-Samardžija Rice University, Chemistry Department, 6100 Main St, Houston, TX 77005, USA and Baker Hughes Incorporateds, 12645 West Airport Blvd, Sugar Land, TX 77478, USA Molecular Structure of Metal Enolates Shmuel Bittner

Ben-Gurion University of the Negev, Department of Chemistry, P. O. Box 653, Beer-Sheva, Israel 84105 Analytical Aspects of Metal Enolates Roy Buschbeck Technische Universität Chemnitz, Fakultät für Naturwissenschaften, Institut für Chemie, Lehrstuhl für Anorganische Chemie, Strasse der Nationen 62, Chemnitz, Germany 09111 Deposition of Metals and Metal Oxides by Means of Metal Enolates Maria Claudia França Cunha Felinto Institute of Nuclear Energy and Research, Av. Prof Lineu Prestes 2242 Cidade Universitária, São Paulo-SP, Brazil 05508-000 Luminescence Phenomena Involving Metal Enolates Paola Deplano Università di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu, Monserrato-Cagliari, Italy I09042 Structure and Properties of d8 Metal–Dithiolene Complexes Luis R. Domingo Universitat de Valencia, Departament de Química Orgánica, Dr. Moliner 50, Valencia, Spain 46100 Burjassot General and Theoretical Aspects of the Metal Enolates Jason Eames University of Hull, Department of Chemistry, Cottingham Road, Kingston upon Hull, England HU6 7RX Acid–Base Properties of Enols and Enolates Ercules Epaminondas de Sousa Teotonio Federal University of Goiás, Department of Chemistry, Av. Dr. Lamartine P. de Avelar, 1120, Catalão-GO, Brazil 75704-020 Luminescence Phenomena Involving Metal Enolates Hermi Felinto Brito University of São Paulo, Department of Fundamental Chemistry, São Paulo-SP, Brazil 05508-000

Luminescence Phenomena Involving Metal Enolates Eli Harlev Ben-Gurion University of the Negev, Department of Chemistry, P. O. Box 653, Beer-Sheva, Israel 84105 Analytical Aspects of Metal Enolates Robert Jérôme University of Liège, Center for Education and Research on Macromolecules (CERM), Sart-Tilman, B6a, Liège, Belgium 4000 Metal Enolates in Polymer Science and Technology Vladislava M. Jovanović University of Belgrade, ICTM-Institute of Electrochemistry, Njegoševa 12, P.O. Box 473, Belgrade, Serbia 11000 Molecular Structure of Metal Enolates Uli Kazmaier Saarland University, Department of Organic Chemistry, D-66123 Saarbrücken, Germany Metal Enolates as Synthons in Organic Chemistry Heinrich Lang Technische Universität Chemnitz, Fakultät für Naturwissenschaften, Institut für Chemie, Lehrstuhl für Anorganische Chemie, Strasse der Nationen 62, Chemnitz, Germany 09111 Deposition of Metals and Metal Oxides by Means of Metal Enolates Philippe Lecomte University of Liège, Center for Education and Research on Macromolecules (CERM), Sart-Tilman, B6a, Liège, Belgium 4000 Metal Enolates in Polymer Science and Technology Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemical Considerations of Metal Enolates Oscar Manoel Loureiro Malta Federal University of Pernambuco, CCEN Cidade Universitária, Department of Fundamental Chemistry, Recife-PE, Brazil 50670-901

Luminescence Phenomena Involving Metal Enolates M. Laura Mercuri Università di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu, Monserrato-Cagliari, Italy I09042 Structure and Properties of d8 Metal–Dithiolene Complexes Li-June Ming University of South Florida, Department of Chemistry and Institute for Biomolecular Science, 4202 E. Fowler Avenue, CHE205, Tampa, FL 33620-5250, USA Biological Aspects of Metal Enolates Guido Pampaloni Università di Pisa, Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126 Redox Chemistry and Electrochemistry of Metal Enolates Luca Pilia Università di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu, Monserrato-Cagliari, Italy I09042 Structure and Properties of d8 Metal–Dithiolene Complexes Katelyn A. Provencher Bates College, Department of Chemistry, Lewiston, ME 04240, USA Lanthanide Enolates as Nuclear Magnetic Resonance Shift Reagents Angela Serpe Università di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu, Monserrato-Cagliari, Italy I09042 Structure and Properties of d8 Metal–Dithiolene Complexes Mitsuru Shindo Kyushu University, Institute for Materials, Chemistry and Engineering, Kasuga-koen, Kasuga, Japan 816-8580

The Chemistry of Metal Ynolates Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA Thermochemical Considerations of Metal Enolates Sofija P. Sovilj University of Belgrade, Faculty of Chemistry, Studentski trg 12-16 P.O. Box 158, Belgrade, Serbia 11000 Molecular Structure of Metal Enolates Daniel Stolz Saarland University, Department of Organic Chemistry, D-66123 Saarbrücken, Germany Metal Enolates as Synthons in Organic Chemistry José Vicente Universidad de Murcia, Grupo de Química Organometálica, Departamento de Química Inorgánica, Facultad de Química, Apdo. 4021, Murcia, Spain 30071 Coordination Chemistry of Metal Enolato Complexes Synthesis of Metal Enolato Complexes Thomas J. Wenzel Bates College, Department of Chemistry, Lewiston, ME 04240, USA Lanthanide Enolates as Nuclear Magnetic Resonance Shift Reagents Stephen A. Westcott Mount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8 Catalysis Using β-Diketonato Metal Complexes Jacob Zabicky Ben-Gurion University of the Negev, Department of Chemical Engineering, P. O. Box 653, Beer-Sheva, Israel 84105 Analytical Aspects of Metal Enolates Piero Zanello

Università di Siena, Dipartimento di Chimica, Via De Gasperi 2, Siena, Italy I-53100 Redox Chemistry and Electrochemistry of Metal Enolates

Organocopper Compounds (2009) Özge Aksin-Artok Dortmund University of Technology, Organic Chemistry II, Otto-Hahn-Strasse 6, Dortmund, Germany D-44227 Copper-Mediated and Copper-Catalyzed Addition and Substitution Reactions of Extended Multiple Bond Systems Alexandre Alexakis University of Geneva, Department of Organic Chemistry, 30, quai Ernest Ansermet 1211 Genève 4, Switzerland Copper-Catalyzed Enantioselective Conjugate Addition Sarah J. Aves University of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, United Kingdom CB2 1EW Oxidation of Organocopper Compounds Asunción Barbero Universidad de Valladolid, Departamento de Química Orgánica, Facultad de Ciencias, Valladolid, Spain 47011 Silyl and Stannyl Derivatives of Organocopper Compounds Donald J. Burton University of Iowa, Department of Chemistry, Iowa City, IA 52242, USA Fluorinated Organocopper Reagents Fabrice Chemla UPMC-Univ Paris 6, Institut Parisien de Chimie Moléculaire, CNRS UMR 7201, Tour 44–45, 2ème Etage, Case 183, 4 Place Jussieu, Paris Cedex 05, France 75252 Carbocupration of Alkynes Charles R. Davis Sigma-Aldrich, 6000 N. Teutonia Avenue, Milwaukee, WI 53209, USA Fluorinated Organocopper Reagents

R. Karl Dieter Clemson University, Howard L. Hunter Laboratory, Department of Chemistry, Clemson, SC 29634-0973, USA N-Functionalized Organocuprates Franck Ferreira UPMC-Univ Paris 6, Institut Parisien de Chimie Moléculaire, CNRS UMR 7201, Tour 44–45, 2ème Etage, Case 183, 4 Place Jussieu, Paris Cedex 05, France 75252 Carbocupration of Alkynes Tobias Gärtner Universität Regensburg, Institut für Organische Chemie, Universitätsstraße 31, Regensburg, Germany D-93040 NMR of Organocopper Compounds Dmitri Gelman The Hebrew University of Jerusalem, Institute of Chemistry, Edmund Safra Campus, Givat Ram, Jerusalem, Israel 91904 Copper-Mediated Cross-Coupling Reactions Saul Gómez-Manzo Universidad Nacional Autónoma de México, Facultad de Química, Ciudad Universitaria, Coyoacán, D.F. México, México 04510 Biochemistry of Organocopper Compounds Ruth M. Gschwind Universität Regensburg, Institut für Organische Chemie, Universitätsstraße 31, Regensburg, Germany D-93040 NMR of Organocopper Compounds Johann T. B. H. Jastrzebski Utrecht University, Chemical Biology & Organic Chemistry, Debye Institute for Nanomaterials Science, Faculty of Science, Padualaan 8, Utrecht, The Netherlands 3584 CH Structural Organocopper Chemistry Jan S. Jaworski University of Warsaw, Faculty of Chemistry, Warszawa, Poland 02-093

Electrochemistry of Organocopper Compounds Gerard van Koten Utrecht University, Chemical Biology & Organic Chemistry, Debye Institute for Nanomaterials Science, Faculty of Science, Padualaan 8, Utrecht, The Netherlands 3584 CH Structural Organocopper Chemistry Norbert Krause Dortmund University of Technology, Organic Chemistry II, Otto-Hahn-Strasse 6, Dortmund, Germany D-44227 Copper-Mediated and Copper-Catalyzed Addition and Substitution Reactions of Extended Multiple Bond Systems Peter M. H. Kroneck Universität Konstanz, Fachbereich Biologie, Konstanz, Germany 78457 Biochemistry of Organocopper Compounds Al Mokhtar Lamsabhi Universidad Autónoma de Madrid, Departamento de Química, Cantoblanco, Madrid, Spain 28049 Gas-Phase Chemistry of Organocopper Compounds Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA Thermochemistry of Organocopper Compounds Eiichi Nakamura The University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan 113-0033 Theory of Organocopper-Mediated Reactions Liza Penn The Hebrew University of Jerusalem, Institute of Chemistry, Edmund Safra Campus, Givat Ram, Jerusalem, Israel 91904

Copper-Mediated Cross-Coupling Reactions Damien Polet University of Geneva, Department of Organic Chemistry, 30, quai Ernest Ansermet 1211 Genève 4, Switzerland Copper-Catalyzed Enantioselective Conjugate Addition Francisco J. Pulido Universidad de Valladolid, Departamento de Química Orgánica, Facultad de Ciencias, Valladolid, Spain 47011 Silyl and Stannyl Derivatives of Organocopper Compounds Olivier Riant Université catholique de Louvain, Unité de chimie organique et médicinale, departement de chimie, Place Louis Pasteur 1, Louvain la Neuve, Belgium 1348 Copper(I) Hydride Reagents and Catalysts Christopher J. Rosenker University of Pittsburgh, Department of Chemistry, Pittsburgh, PA 15260, USA Transmetalation Reactions Producing Organocopper Compounds Jean-Yves Salpin Université d'Evry Val d'Essonne, Laboratoire d'Analyse et Modélisation pour la Biologie et l'Environnement-CNRS, UMR 8587—Bâtiment Maupertuis, Boulevard François Mitterrand, Evry, France 91025 Gas-Phase Chemistry of Organocopper Compounds Juan P. Saucedo-Vázquez Universidad Nacional Autónoma de México, Facultad de Química, Ciudad Universitaria, Coyoacán, D.F. México, México 04510 Biochemistry of Organocopper Compounds Mathias O. Senge Trinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland and St. James's Hospital, Trinity College Dublin, Institute of Molecular Medicine, Medicinal Chemistry, Trinity Centre for Health Sciences, Dublin 8, Ireland Photochemical Transformations Involving Copper Porphyrins and Phthalocyanines

Natalia N. Sergeeva Trinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland Photochemical Transformations Involving Copper Porphyrins and Phthalocyanines Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA Thermochemistry of Organocopper Compounds Martha E. Sosa-Torres Universidad Nacional Autónoma de México, Facultad de Química, Ciudad Universitaria, Coyoacán, D.F. México, México 04510 Biochemistry of Organocopper Compounds Claude Spino Université de Sherbrooke, Département de Chimie, Sherbrooke, Québec, Canada J1K 2R1 Copper-Mediated Asymmetric Allylic Alkylations David R. Spring University of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, United Kingdom CB2 1EW Oxidation of Organocopper Compounds Jeanine Tortajada Université d'Evry Val d'Essonne, Laboratoire d'Analyse et Modélisation pour la Biologie et l'Environnement-CNRS, UMR 8587—Bâtiment Maupertuis, Boulevard François Mitterrand, Evry, France 91025 Gas-Phase Chemistry of Organocopper Compounds Rhett T. Watson University of South Carolina Upstate, Division of Natural Sciences and Engineering, 800 University Way, Spartanburg, SC 29303, USA N-Functionalized Organocuprates Peter Wipf University of Pittsburgh, Department of Chemistry, Pittsburgh, PA 15260, USA

Transmetalation Reactions Producing Organocopper Compounds Manuel Yáñez Universidad Autónoma de Madrid, Departamento de Química, Cantoblanco, Madrid, Spain 28049 Gas-Phase Chemistry of Organocopper Compounds Naohiko Yoshikai The University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan 113-0033 Theory of Organocopper-Mediated Reactions

Hydroxylamines, Oximes and Hydroxamic Acids (2010) Edgars Abele Latvian Institute of Organic Synthesis, Riga, LV1006, Latvia Synthesis, structure and reactions of organometallic derivatives of oximes Fernando Albericio Institute for Research in Biomedicine, Barcelona Science Park, Baldiri Reixac 10, 08028-Barcelona, Spain, Biomaterials and Nanomedicine, CIBER-BBN, Networking Centre on Bioengineering, Barcelona Science Park, Baldiri Reixac 10, 08028-Barcelona, Spain and University of Barcelona, Martí i Franqués 1-11, Department of Organic Chemistry, 08028-Barcelona, Spain N-Hydroxylamines for peptide synthesis Concepción Alonso Facultad de Farmacia, Universidad del País Vasco, Departamento de Química Orgánica I, Apartado 450, 01080 Vitoria Spain Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acids John E. Bartmess University of Tennessee, Department of Chemistry, Knoxville, TN 37996 1600, USA The Brønsted acid/base character of hydroxylamines, oximes and hydroxamic acids

Carlos D. Bravo-díaz Universidad de Vigo, Fac. Química, Dpto. Química, Física, 36 310 Vigo, Pontevedra, Spain Diazohydroxides, diazoethers and related species Mrinal Chakraborty Miami University, Department of Chemistry and Biochemistry, Oxford, OH 45056, USA N-Arylhydroxylamines and chemical carcinogenicity Renata Dreos Università degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy Properties, structure and reactivity of cobaloximes Yunfei Du School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin, Peoples’ Republic of China 300072 Conjugate addition of hydroxylamines, oximes and hydroxamic acids Ayman El-Faham Alexandria University, Faculty of Science, Department of Chemistry, P.O. Box 246, Ibrahimia, 21321 Alexandria, Egypt N-Hydroxylamines for peptide synthesis Anthony S. Evans Johns Hopkins University, Department of Chemistry, Baltimore, MD 21218, USA The chemistry of NO- and HNO-producing diazeniumdiolates Silvano Geremia Università degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy Properties, structure and reactivity of cobaloximes Gianluca Giorgi Department of Chemistry, University of Siena, Via Aldo Moro I-53100 Siena, Italy Mass spectrometry of hydroxylamines, oximes and hydroxamic acids

Alexander Greer Department of Chemistry, Graduate Center and CUNY, Brooklyn College, 2900 Bedford Ave., Brooklyn, NY 11210, USA Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bonding Martins Katkevics Latvian Institute of Organic Synthesis, Riga, Latvia LV1006 Heterocycles from hydroxylamines and hydroxamic acids Naoshi Kojima Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 2-17-2-1 Tsukisamu-Higashi, Toyohira-ku, Sapporo 062-8517, Japan Hydroxylamine, oxime and hydroxamic acid derivatives of nucleic acids Yasuo Komatsu Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 2-17-2-1 Tsukisamu-Higashi, Toyohira-ku, Sapporo 062-8517, Japan Hydroxylamine, oxime and hydroxamic acid derivatives of nucleic acids Tatyana Kukosha Latvian Institute of Organic Synthesis, Riga, Latvia LV1006 Heterocycles from hydroxylamines and hydroxamic acids Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bonding Edmunds Lukevics Latvian Institute of Organic Synthesis, Riga, LV1006, Latvia Heterocycles from hydroxylamines and hydroxamic acids Synthesis, structure and reactions of organometallic derivatives of oximes Antonello Mai Sapienza University of Rome, Pasteur Institute—Cenci Bolognetti Foundation, Department of Drug Chemistry and Technologies, P.le A. Moro 5, 00185 Rome, Italy

Hydroxamic acids: Biological properties and potential uses as therapeutic agents Deng Mao School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin, Peoples’ Republic of China 300072 Conjugate addition of hydroxylamines, oximes and hydroxamic acids Michael Novak Miami University, Department of Chemistry and Biochemistry, Oxford, OH 45056, USA N-Arylhydroxylamines and chemical carcinogenicity Francisco Palacios Facultad de Farmacia, Universidad del País Vasco, Departamento de Química Orgánica I, Apartado 450, 01080 Vitoria Spain Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acids Lucio Randaccio Università degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy Properties, structure and reactivity of cobaloximes Heinz D. Roth Rutgers University, Department of Chemistry and Chemical Biology, New Brunswick, NJ 08854 0939, USA Light-induced chemistry of oximes and derivatives Jesús M. de los Santos Facultad de Farmacia, Universidad del País Vasco, Departamento de Química Orgánica I, Apartado 450, 01080 Vitoria Spain Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acids Patrizia Siega Università degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy Properties, structure and reactivity of cobaloximes Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA

Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bonding Ramon Subirós-Funosas Institute for Research in Biomedicine, Barcelona Science Park, Baldiri Reixac 10, 08028-Barcelona, Spain N-Hydroxylamines for peptide synthesis John P. Toscano Johns Hopkins University, Department of Chemistry, Baltimore, MD 21218, USA The chemistry of NO- and HNO-producing diazeniumdiolates Javier Vicario Facultad de Farmacia, Universidad del País Vasco, Departamento de Química Orgánica I, Apartado 450, 01080 Vitoria Spain Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acids Daisy Zhang-Negrerie School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin, Peoples’ Republic of China 300072 Conjugate addition of hydroxylamines, oximes and hydroxamic acids Kang Zhao School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin, Peoples’ Republic of China 300072 Conjugate addition of hydroxylamines, oximes and hydroxamic acids Gury Zvilichovsky Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel Hydroxylamine analogs and derivatives of amino acids. Aminooxy acids

Organomanganese Compounds (2011) Noam Adir

Schulich Faculty of Chemistry, Technion—Israel Institute of Technology, Haifa, Israel 32000 Manganese in Biological Systems: Transport and Function Gérard Cahiez Laboratoire de Synthèse Organique Sélective et de Chimie Organométallique (SOSCOM), FRE 3043 CNRS-Université Paris13, 74 rue Marcel Cachin, Bobigny, France F-93017 Preparation and Reactivity of Organomanganese Compounds Nicka Chinkov Faculty of Natural Sciences, Department of Biology and Environment, University of Haifa, Oranim, Kiryat Tivon, Israel 36006 Catalytic Enantioselective Reactions using Organomanganese Compounds José M. Concellón Universidad de Oviedo, Departamento de Química Orgánica e Inorgánica, Facultad de Química, Julián Clavería 8, Oviedo, Spain 33 071 The Chemistry of Manganese Enolates Vicente Del Amo Universidad de Oviedo, Departamento de Química Orgánica e Inorgánica, Facultad de Química, Julián Clavería 8, Oviedo, Spain 33 071 The Chemistry of Manganese Enolates Antoine Eloi Université Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de Chimie Organique et Organométallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252 Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesis and Reactivity Gregory K. Friestad University of Iowa, Department of Chemistry, Iowa City, IA 52 242, USA Organomanganese-Mediated Radical Reactions Olivier Gager Laboratoire de Synthèse Organique Sélective et de Chimie Organométallique (SOSCOM), FRE 3043 CNRS-Université Paris13, 74 rue Marcel Cachin, Bobigny, France F-93017

Preparation and Reactivity of Organomanganese Compounds Timothy P. Hanusa Vanderbilt University, Department of Chemistry, Nashville, TN 37235, USA Structural Organomanganese Chemistry Margarita Kanteev Schulich Faculty of Chemistry, Technion—Israel Institute of Technology, Haifa, Israel 32000 Manganese in Biological Systems: Transport and Function Nir Keren Department of Plant and Environmental Sciences, Silberman Institute of Life sciences, The Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat-Ram, Jerusalem, Israel 91904 Manganese in Biological Systems: Transport and Function Richard A. Layfield The University of Manchester, School of Chemistry, Oxford Road, Manchester, UK M13 9PL s-Block-Metal-Mediated Manganation Reactions Donald G. Lee University of Regina, Department of Chemistry and Biochemistry, Regina, Saskatchewan, Canada S4S 1P2 Structures and Reaction Mechanisms of Manganese Oxidants Jerzy Leszczynski Department of Chemistry and Interdisciplinary Center for Nanotoxicity, Jackson State University, Jackson, MS 39217, USA Structure and Bonding of Simple Manganese-Containing Compounds Joel F. Liebman University of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore, MD 21250, USA

Energetics of Organomanganese Compounds Devashis Majumdar Department of Chemistry and Interdisciplinary Center for Nanotoxicity, Jackson State University, Jackson, MS 39217, USA Structure and Bonding of Simple Manganese-Containing Compounds Ryan M. Meier Vanderbilt University, Department of Chemistry, Nashville, TN 37235, USA Structural Organomanganese Chemistry Minh Tho Nguyen Department of Chemistry, Katholieke Universiteit Leuven, B-3001 Leuven, Belgium Structure and Bonding of Simple Manganese-Containing Compounds Koichiro Oshima Kyoto University, Department of Material Chemistry, Graduate School of Engineering, Kyoto-daigaku Katsura, Nishikyo-ku, Kyoto, Japan 615-8510 The Chemistry of Organomanganese Ate Complexes Sergiu P. Palii University of Florida, Biomedical Mass Spectrometry Laboratory, Clinical Research Center, Gainesville, FL 32610 0322, USA Mass Spectrometry and Gas-Phase Ion Chemistry of Organomanganese Complexes Humberto Rodríguez-Solla Universidad de Oviedo, Departamento de Química Orgánica e Inorgánica, Facultad de Química, Julián Clavería 8, Oviedo, Spain 33 071 The Chemistry of Manganese Enolates Eric Rose Université Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de Chimie Organique et Organométallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252 Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesis and Reactivity

Françoise Rose-Munch Université Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de Chimie Organique et Organométallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252 Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesis and Reactivity Szczepan Roszak Institute of Physical and Theoretical Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland Structure and Bonding of Simple Manganese-Containing Compounds Eitan Salomon Department of Plant and Environmental Sciences, Silberman Institute of Life sciences, The Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat-Ram, Jerusalem, Israel 91904 Manganese in Biological Systems: Transport and Function Suzanne W. Slayden Department of Chemistry George Mason University, 4400 University Drive, Fairfax, VA 22030, USA Energetics of Organomanganese Compounds Hideki Yorimitsu Kyoto University, Department of Chemistry, Graduate School of Science, Kitashirakawa, Sakyo-ku, Kyoto, Japan 606-8502 The Chemistry of Organomanganese Ate Complexes Dmitri V. Zagorevskii Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, 1145 CBIS, 110 8th Str., Troy, NY 12180, USA Mass Spectrometry and Gas-Phase Ion Chemistry of Organomanganese Complexes

Organic Selenium and Tellurium Compounds (2012)

Thomas G. Back University of Calgary, Department of Chemistry, Calgary, Alberta, Canada, T2N 1N4 Advances in Free Radical Reactions of Organoselenium and Organotellurium Compounds Joris Beld Laboratory of Organic Chemistry, ETH Zürich, Zürich, Switzerland The Chemistry of Selenocysteine Michael Bendikov Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100 Selenium- and Tellurium-Containing Organic π-Conjugated Oligomers and Polymers Michael R. Detty Department of Chemistry, University at Buffalo, Buffalo, NY 14260 3000, USA Biological and Biochemical Aspects of Tellurium Derivatives Józef Drabowicz Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland and Jan Dlugosz University in Czestochowa, Department of Chemistry, Environment Protection and Biotechnology, 42-200-Czestochowa, Armii Krajowej Ave. 13/15, Poland Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6 Hypervalent Derivatives of Selenium and Tellurium Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and Derivatives Gauthier Eppe Inorganic Analytical Chemistry, University of Liège, 3, Laboratory of Mass Spectrometry, Allée de la Chimie B6C, Liège, Belgium 4000 Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium and Tellurium Compounds Johann Far Inorganic Analytical Chemistry, University of Liège, 3, Laboratory of Mass Spectrometry, Allée de la Chimie B6C, Liège, Belgium 4000

Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium and Tellurium Compounds Donald Hilvert Laboratory of Organic Chemistry, ETH Zürich, Zürich, Switzerland The Chemistry of Selenocysteine Jan S. Jaworski Faculty of Chemistry, University of Warsaw, Warszawa, Poland 02-093 Electrochemistry of Organic Selenium and Tellurium Compounds Thomas M. Klapötke Ludwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5-13(D), D-81377 Munich, Germany Compounds of Selenium and Tellurium with Nitrogen Bonds Piotr Kiełbasiński Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6 Hypervalent Derivatives of Selenium and Tellurium Dorota Krasowska Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, Lodz, Poland 90-363 Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and Derivatives Burkhard Krumm Ludwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5-13(D), D-81377 Munich, Germany Compounds of Selenium and Tellurium with Nitrogen Bonds Joel F. Liebman

University of Maryland, Baltimore County (UMBC), Department of Chemistry and Biochemistry, 1000 Hilltop Circle, Baltimore MD 21250, USA Aspects of the Chemistry of Species with Carbon–Polonium Bonds Thermochemistry of Organoselenium and Organotellurium Compounds Rafał Lisiak Wrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, Wybrzeże Wyspiańskiego 27, Wrocław, Poland 50 370 Organoselenium and Organotellurium Oxidation and Reduction Margaret E. Logan The College at Brockport, Department of Chemistry, SUNY, Brockport, NY 14420, USA Substituent Constants and Substituent Effects in Organoselenium and Organotellurium Compounds Ricardo L. Longo Universidade Federal de Pernambuco, Cidade Universitária, Departamento de Química Fundamental, Recife, PE, Brazil 50740-540 Theoretical and Computational Aspects of Organotellurium Compounds Paulo H. Menezes Universidade Federal de Pernambuco, Cidade Universitária, Departamento de Química Fundamental, Recife, PE, Brazil 50740-540 Theoretical and Computational Aspects of Organotellurium Compounds Paulo Henrique Menezes Universidade Federal de Pernambuco, Departamento Química Fundamental, Recife, PE, Brazil 50670-901 Vinyl Selenides Vinylic Tellurides Norman Metanis Laboratory of Organic Chemistry, ETH Zürich, Zürich, Switzerland The Chemistry of Selenocysteine Wanda H. Midura

Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6 Wanda Halina Midura Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, Lodz, Poland 90-363 Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and Derivatives Jacek Młochowski Wrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, Wybrzeże Wyspiańskiego 27, Wrocław, Poland 50 370 Organoselenium and Organotellurium Oxidation and Reduction Richard Moll Ludwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5-13(D), D-81377 Munich, Germany Compounds of Selenium and Tellurium with Nitrogen Bonds Yasuyuki Nakamura Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan 611-0011 Organotellurium Compounds as Chain Transfer agents for Living Radical Polymerization Cristina W. Nogueira Laboratório de Síntese, Reatividade e Avaliacão Farmacológica e Toxicológica de Organocalcogênios, CCNE, UFSM, Santa Maria, RS, Brazil CEP 97105-900 Organoselenium and organotellurium compounds: Toxicology and pharmacology Akihiro Nomoto Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Department of Applied Chemistry, Naka-ku, Sakai, Osaka 599-8531, Japan Preparative Uses of Organoselenium and Organotellurium Compounds Akiya Ogawa Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Department of Applied Chemistry, Naka-ku, Sakai, Osaka 599-8531, Japan

Preparative Uses of Organoselenium and Organotellurium Compounds Asit Patra Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100 Selenium- and Tellurium-Containing Organic π-Conjugated Oligomers and Polymers Edwin De Pauw Inorganic Analytical Chemistry, University of Liège, 3, Laboratory of Mass Spectrometry, Allée de la Chimie B6C, Liège, Belgium 4000 Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium and Tellurium Compounds Maja Ponikvar-Svet Jožef Stefan Institute,, Department of Inorganic Chemistry and Technology, Jamova 39, SI-1000 Ljubljana, Slovenia Aspects of the Chemistry of Species with Carbon–Polonium Bonds David J. Press University of Calgary, Department of Chemistry, Calgary, Alberta, Canada, T2N 1N4 Advances in Free Radical Reactions of Organoselenium and Organotellurium Compounds João B. T. Rocha Laboratório de Síntese, Reatividade e Avaliacão Farmacológica e Toxicológica de Organocalcogênios, CCNE, UFSM, Santa Maria, RS, Brazil CEP 97105-900 Organoselenium and organotellurium compounds: Toxicology and pharmacology Fateh V. Singh School of Chemistry, Cardiff University, Park Place, Cardiff, UK CF10 3AT Stereoselective Reactions of Organoselenium Reagents Including Catalysis Suzanne W. Slayden George Mason University, Department of Chemistry, 4400 University Drive, Fairfax VA 22030, USA Thermochemistry of Organoselenium and Organotellurium Compounds Raghavan B. Sunoj Indian Institute of Technology Bombay, Department of Chemistry, Powai, Mumbai, India 400076

Theoretical Aspects of Organoselenium Chemistry Thomas Wirth School of Chemistry, Cardiff University, Park Place, Cardiff, UK CF10 3AT Stereoselective Reactions of Organoselenium Reagents Including Catalysis Halina Wójtowicz-Młochowska Wrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, Wybrzeże Wyspiańskiego 27, Wrocław, Poland 50 370 Organoselenium and Organotellurium Oxidation and Reduction Shigeru Yamago Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan 611-0011 Organotellurium Compounds as Chain Transfer agents for Living Radical Polymerization Adrian Zajac Polish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Sienkiewicza 112, Lodz, Poland 90-363 Hypervalent Derivatives of Selenium and Tellurium Gilson Zeni Universidade Federal de Santa Maria, Departamento de Química, Santa Maria, RS, Brazil 97105-900 Vinyl Selenides Vinylic Tellurides

Metal Phenolates (2013) Jerry L. Atwood Department of Chemistry, University of Missouri, Columbia, Missouri 65211-8600, USA Molecular Capsules Based on Metal Complexes with Resorcin[4]arenes and Pyrogallol[4]arenes Fernando H. Bartoloni Centro de Ciências Naturais e Humanas, Universidade Federal do ABC. Rua Santa Adélia, 166, Bloco A, S627-3, 09210-170 Santo André, SP, Brazil

Acid–Base and Solvation Properties of Metal Phenolates Erick L. Bastos Instituto de Química, Universidade de São Paulo. Av. Prof. Lineu Prestes, 748, Bloco 4 Sup., S460, 05508-000 São Paulo, SP, Brazil Acid–Base and Solvation Properties of Metal Phenolates Stéphane Bellemin-Laponnaz Institut de Physique et Chimie des Matériaux de Strasbourg, Université de Strasbourg-CNRS, 23 rue du Loess, 67034 Strasbourg cedex 2, France Coordination Chemistry and Applications of Salen, Salan and Salalen Metal Complexes Jean-François Carpentier Organometallics, Materials and Catalysis laboratories, Institut des Sciences Chimiques de Rennes, UMR 6226 CNRS-University of Rennes 1, 35042 Rennes Cedex, France Metal Phenolates as Polymerization Catalysts Renzo Cini Università di Siena, Dipartimento di Biotecnologie, Chimica e Farmacia, Via Alcide de Gasperi 2, I-53100 Siena, Italy Biomimetic Metal Phenolates Maddalena Corsini Università di Siena, Dipartimento di Biotecnologie, Chimica e Farmacia, Via Aldo Moro 2, I-53100 Siena, Italy Redox Chemistry and Electrochemistry of Homoleptic Metal Phenolates Samuel Dagorne Institut de Chimie, Université de Strasbourg-CNRS, 1 rue Blaise Pascal, 67000 Strasbourg, France Coordination Chemistry and Applications of Salen, Salan and Salalen Metal Complexes Carol A. Deakyne Department of Chemistry, University of Missouri, Columbia, Missouri 65211-8600, USA Molecular Capsules Based on Metal Complexes with Resorcin[4]arenes and Pyrogallol[4]arenes Linda H. Doerrer

Department of Chemistry, Boston University, Boston, MA 02215, USA Coordination Chemistry of Metal Phenolates—General Aspects Maria Elisa da Silva Serra Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra, Portugal Catalysis of Organic Processes by Metal Phenolates Fabrizia Fabrizi de Biani Università di Siena, Dipartimento di Biotecnologie, Chimica e Farmacia, Via Aldo Moro 2, I-53100 Siena, Italy Redox Chemistry and Electrochemistry of Homoleptic Metal Phenolates Drew A. Fowler Department of Chemistry, University of Missouri, Columbia, Missouri 65211-8600, USA Molecular Capsules Based on metal Complexes with Resorcin[4]arenes and Pyrogallol[4]arenes LetíCia C. P. Gonçalves Centro de Ciências Naturais e Humanas, Universidade Federal do ABC. Rua Santa Adélia, 166, Bloco A, S627-3, 09210-170 Santo André, SP, Brazil Acid–Base and Solvation Properties of Metal Phenolates Tracy A. Hanna Texas Christian University, Fort Worth, TX 76129, USA Coordination Chemistry and Applications of Phenolic Calixarene–Metal Complexes Constantin M. Indricean Institute of Chemistry, Academy of Sciences of the Republic of Moldova, Academiei Str. 3, Chişinău, MD-2028, Republic of Moldova Mass Spectrometry and Gas-phase Ion Chemistry of Metal–phenolate and Metal–phenol complexes Joseph K. Kelly Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0215, USA Coordination Chemistry of o-semiquinones Berthold Kersting

Institut für Anorganische Chemie, Universität Leipzig, Johannisallee 29, D-04103 Leipzig, Germany The Chemistry of Metal Thiophenolates Evgeny Kirillov Organometallics, Materials and Catalysis laboratories, Institut des Sciences Chimiques de Rennes, UMR 6226 CNRS-University of Rennes 1, 35042 Rennes Cedex, France Metal Phenolates as Polymerization Catalysts Julia Klingele Institut für Anorganische und Analytische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstr. 21, D-79104 Freiburg, Germany The Chemistry of Metal Thiophenolates Marco H. Klingele Losan Pharma GmbH, Ott-Hahn-Strasse 13, D-79395 Neuenburg, Germany The Chemistry of Metal Thiophenolates Yuanzhou Li Sichuan Normal University, Chengdu 61006, China Coordination Chemistry and Applications of Phenolic Calixarene–Metal Complexes Giulia Licini Dipartimento di Scienze Chimiche, Università degli studi di Padova, via Marzolo, 1, I-35131 Padova, Italy Coordination Chemistry and Applications of Nitrilotris(N-methylenephenoxy)–metal Complexes Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, USA The Experimental Thermochemistry of Metal Phenolates Miriam Mba Dipartimento di Scienze Chimiche, Università degli studi di Padova, via Marzolo, 1, I-35131 Padova, Italy Coordination Chemistry and Applications of Nitrilotris(N-methylenephenoxy)–metal Complexes

Li-June Ming Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE205, Tampa, Florida 33620, USA Biological and Biomedical Aspects of Metal Phenolates Dina M. B. Murtinho Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra, Portugal Catalysis of Organic Processes by Metal Phenolates Alane Y. Nuñez Texas Christian University, Fort Worth, TX 76129, USA Coordination Chemistry and Applications of Phenolic Calixarene–metal Complexes Bernat A. Martínez Ortega Department of Chemistry, Geosciences, and Physics, Tarleton State University, Stephenville, TX 76402, USA Coordination Chemistry and Applications of Phenolic Calixarene–metal Complexes Sergiu P. Palii Biomedical Mass Spectrometry Laboratory, Clinical Research Center, University of Florida, Gainesville, FL 32610-0322, USA Mass Spectrometry and Gas-Phase Ion Chemistry of Metal–phenolate and Metal–phenol Complexes Cortlandt G. Pierpont Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0215, USA Coordination Chemistry of o-semiquinones Carl Redshaw University of Hull, Cottingham Road, Hull, HU6 7RX, England Coordination Chemistry and Applications of Phenolic Calixarene–metal Complexes Mihail D. Revenco

Department of Chemistry and Chemical Technology, Moldova State University, Alexei Mateevici Str. 60, Chişinău, MD-2009, Republic of Moldova Mass Spectrometry and Gas-Phase Ion Chemistry of Metal–phenolate and Metal–phenol Complexes Yann Sarazin Organometallics, Materials and Catalysis laboratories, Institut des Sciences Chimiques de Rennes, UMR 6226 CNRS-University of Rennes 1, 35042 Rennes Cedex, France Metal Phenolates as Polymerization Catalysts Yuichi Shimazaki College of Science, Ibaraki University, Bunkyo, Mito 310-8512, Japan Phenoxyl Radical–metal Complexes Suzanne W. Slayden Department of Chemistry and Biochemistry, George Mason University, 4400 University Drive, Fairfax, Virginia 22030, USA The Experimental Thermochemistry of Metal Phenolates Gabriella Tamasi Università di Siena, Dipartimento di Biotecnologie, Chimica e Farmacia, Via Alcide de Gasperi 2, I-53100 Siena, Italy Biomimetic Metal Phenolates Jacob Zabicky Department of Chemical Engineering, Ben-Gurion University of the Negev, P. O. Box 653, Beer-Sheva 84105, Israel Analytical Aspects of Metal Phenolates Piero Zanello Università di Siena, Dipartimento di Biotecnologie, Chimica e Farmacia, Via Aldo Moro 2, I-53100 Siena, Italy Redox Chemistry and Electrochemistry of Homoleptic Metal Phenolates Ke-Qing Zhao Sichuan Normal University, Chengdu 61006, China

Coordination Chemistry and Applications of Phenolic Calixarene–metal Complexes Cristiano Zonta Dipartimento di Scienze Chimiche, Università degli studi di Padova, via Marzolo, 1, I-35131 Padova, Italy Coordination Chemistry and Applications of Nitrilotris(N-methylenephenoxy)–metal Complexes

Organic Selenium and Tellurium (2013) Wataru Ando Research Institute for Innovation in Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8565, Japan. Advances in the Photochemistry of Organoselenium and Organotellurium Compounds Maria Carla Aragoni Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Cagliari, S.S. 554 Bivio per Sestu, 09042 Monserrato (CA), Italy. Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Massimiliano Arca Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Cagliari, S.S. 554 Bivio per Sestu, 09042 Monserrato (CA), Italy. Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Debasish Bhowmick Indian Institute of Science, Department of Inorganic & Physical Chemistry, Bangalore 560 012, India. Enzyme Mimetic Chemistry of Organoselenium Compounds Antonio L. Braga LabSelen – Laboratório de Síntese de Pequenas Moléculas Quirais de Selênio e Telúrio, Dpto de Química – CFM, UFSC – Florianópolis, CEP 88040-900, SC – Brazil. Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part A. Antioxidant Compounds

Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part C. Miscellaneous Biological Activities Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part B. Anti-infective and Anticancer Compounds Ignez Caracelli BioMat, Departamento de Física, Universidade Federal de São Carlos, C.P. 676, São Carlos, São Paulo, 13565-905, Brazil. Supramolecular Architectures Based on M(lone pair)…π(arene) Interactions for M═Se and Te João V. Comasseto Instituto de Química, Departamento de Química Fundamental, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, 05508-000, São Paulo/SP, Brazil. and Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Av. Prof. Artur Riedel, 275, 09972-270, Diadema/SP, Brazil. Synthesis of Selenium and Tellurium Ylides and Carbanions. Application to Organic Synthesis Michael R. Detty University at Buffalo, Buffalo, NY 14260-3000, USA. Selenium and Tellurium Heterocycles Piotr Guga Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Bioorganic Chemistry, Sienkiewicza Str. 112, 90-363 Łódź, Poland. Selenium and Tellurium Derivatives of Carbohydrates and Nucleotides Frank S. Guziec, Jr. Department of Chemistry and Biochemistry, Southwestern University, Georgetown, TX 78626, USA. Recent Advances in the Insertion and Extrusion Reactions of Selenium and Tellurium in Organic Compounds Lynn James Guziec

Department of Chemistry and Biochemistry, Southwestern University, Georgetown, TX 78626, USA. Recent Advances in the Insertion and Extrusion Reactions of Selenium and Tellurium in Organic Compounds Janet E. Hack Reference Department, Albin O. Kuhn Library and Gallery, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA. A Summary of Functional Groups Containing Selenium and Tellurium: A Catalog of the Many Groups that are Known and Some that are Not Ionel Haiduc Facultatea de Chimie, Universitatea Babes-Bolyai, RO-400028 Cluj-Napoca, Romania. Supramolecular Architectures Based on M(lone pair)…π(arene) Interactions for M═Se and Te Masato Hashimoto Department of Material Science and Chemistry, Faculty of Systems Engineering, Wakayama University, 930 Sakaedani, Wakayama 640-8510, Japan. Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Satoko Hayashi Department of Material Science and Chemistry, Faculty of Systems Engineering, Wakayama University, 930 Sakaedani, Wakayama 640-8510, Japan. Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Meredith A. Lang University at Buffalo, Buffalo, NY 14260-3000, USA. Selenium and Tellurium Heterocycles Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA. A Summary of Functional Groups Containing Selenium and Tellurium: A Catalog of the Many Groups that are Known and Some that are Not

Vito Lippolis Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Cagliari, S.S. 554 Bivio per Sestu, 09042 Monserrato (CA), Italy. Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Margaret E. Logan Department of Chemistry, SUNY College at Brockport, Brockport, NY 14420, USA. Selenium and Tellurium Heterocycles Anna Maciaszek Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Bioorganic Chemistry, Sienkiewicza Str. 112, 90-363 Łódź, Poland. Selenium and Tellurium Derivatives of Carbohydrates and Nucleotides Govindasamy Mugesh Indian Institute of Science, Department of Inorganic & Physical Chemistry, Bangalore 560 012, India. Enzyme Mimetic Chemistry of Organoselenium Compounds Toshiaki Murai Department of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu, 501-1193, Japan. Organic Compounds Containing Bonds between Se or Te with P, As, Sb and Bi Rearrangements of Organoselenium and Organotellurium Compounds Yuichiro Mutoh Department of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. Coordination Chemistry of Organoselenium and Organotellurium Compounds Waro Nakanishi Department of Material Science and Chemistry, Faculty of Systems Engineering, Wakayama University, 930 Sakaedani, Wakayama 640-8510, Japan.

Recent Advances of Structural Chemistry of Organoselenium and Organotellurium Compounds Osamu Niyomura Department of Applied Chemistry, College of Engineering, Chubu University, Matsumoto-cho, Kasugai, Aichi, 487-8501, Japan. Rearrangements of Organoselenium and Organotellurium Compounds Makoto Oba Department of Materials Chemistry, Tokai University, Numazu, Shizuoka 410-0395, Japan. Advances in the Photochemistry of Organoselenium and Organotellurium Compounds Akihiko Ouchi Research Institute for Innovation in Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8565, Japan. Advances in the Photochemistry of Organoselenium and Organotellurium Compounds Arunashree Panda Department of Chemistry, Birla Institute of Technology and Science, Pilani – K. K. Birla Goa Campus, Goa – 403726, India. NMR of Organoselenium and Organotellurium Compounds Leandro Piovan Departamento de Química, Universidade Federal do Paraná, Rua Cel. Francisco Heráclito dos Santos, 100, 81531-980, Curitiba/PR, Brazil. Synthesis of Selenium and Tellurium Ylides and Carbanions. Application to Organic Synthesis Vladimir A. Potapov A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., RUS-664033 Irkutsk, Russian Federation. Organic Diselenides, Ditellurides, Polyselenides and Polytellurides. Synthesis and Reactions Jamal Rafique LabSelen – Laboratório de Síntese de Pequenas Moléculas Quirais de Selênio e Telúrio, Dpto de Química – CFM, UFSC – Florianópolis, CEP 88040-900, SC – Brazil.

Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part A. Antioxidant Compounds Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part C. Miscellaneous Biological Activities Synthesis of Biologically Relevant Small Molecules Containing Selenium. Part B. Anti-infective and Anticancer Compounds Claudio Santi Department of Chemistry and Technology of Drugs, Group of Catalysis and Green Chemistry, University of Perugia, Via del Liceo 1, 06134 Perugia, Italy. Electrophilic Selenium/Tellurium Reagents: Reactivity and their Contribution to Green Chemistry Soichi Sato Department of Chemistry, Tokyo Metropolitan University, Minami-ohsawa, Hachioji, Tokyo 192-0397, Japan. Positively Charged Selenium- and Tellurium-Stabilized Species Harkesh B. Singh Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai-400076, India. NMR of Organoselenium and Organotellurium Compounds Synthesis of Organoselenium Compounds Synthesis of Organotellurium Compounds Peter J. Skabara WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, G1 1XL, Glasgow, UK. Organic Conductors Containing Selenium and Tellurium Caterina Tidei

Department of Chemistry and Technology of Drugs, Group of Catalysis and Green Chemistry, University of Perugia, Via del Liceo 1, 06134 Perugia, Italy. Electrophilic Selenium/Tellurium Reagents: Reactivity and their Contribution to Green Chemistry Edward R. T. Tiekink Department of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia. Supramolecular Architectures Based on M(lone pair)…π(arene) Interactions for M═Se and Te Agnieszka Tomaszewska Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Bioorganic Chemistry, Sienkiewicza Str. 112, 90-363 Łódź, Poland. Selenium and Tellurium Derivatives of Carbohydrates and Nucleotides Akio Toshimitsu Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan. Organic Selenocyanates, Tellurocyanates and Related Compounds Filipe Vilela Max Planck Institute of Colloids and Interfaces, Department of Colloid Chemistry, Research Campus Golm, D-14424, Potsdam, Germany. Organic Conductors Containing Selenium and Tellurium Zuzana Vobecka Max Planck Institute of Colloids and Interfaces, Department of Colloid Chemistry, Research Campus Golm, D-14424, Potsdam, Germany. Organic Conductors Containing Selenium and Tellurium Edison P. Wendler Instituto de Química, Departamento de Química Fundamental, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, 05508-000, São Paulo/SP, Brazil.

Synthesis of Selenium and Tellurium Ylides and Carbanions. Application to Organic Synthesis Sanjio S. Zade Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, PO: BCKV campus main office, Mohanpur 741252, Nadia, West Bengal, India. Synthesis of Organoselenium Compounds Synthesis of Organotellurium Compounds Julio Zukerman-Schpector Laboratório de Cristalografia, Estereodinâmica e Modelagem Molecular, Departamento de Química, Universidade Federal de São Carlos, C.P. 676, São Carlos, SP, 13565-905, Brazil. Supramolecular Architectures Based on M(lone pair)…π(arene) Interactions for M═Se and Te

Organoiron Compounds (2013) Eduardo Alberch Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, 3210 N Cramer St, Milwaukee WI 53211, USA The Chemistry of Iron–Alkyl Complexes MD. Sharif Asad Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, 3210 N Cramer St, Milwaukee WI 53211, USA The Chemistry of Iron–Alkyl Complexes Ingmar Bauer Department Chemie, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany The Chemistry of Diene–Iron and Dienyl–Iron Complexes Jean-Marc Campagne Institut Charles Gerhardt UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l&apos;Ecole Normale, 34296 Montpellier Cedex 5, France

Organic Transformations Promoted by Lewis Acid Iron Catalysts Arada Chaiyanurakkul Department of Chemistry, Faculty of Science, Mahidol University, Ratchathewi, Bangkok 10400, Thailand Iron-promoted Reduction Reactions Karine Costuas Sciences Chimiques de Rennes, UMR CNRS 6226, Université de Rennes 1, Campus de Beaulieu, 35042 Rennes, Cedex, France Theory of Ferrocenyl Compounds Etienne Derat Institut Parisien de Chimie Moléculaire, UMR CNRS 7201, UPMC, Sorbonne Universités, 75005 Paris, France Theory of Ferrocenyl Compounds Gerhard Erker Organisch-Chemisches Institut, Universität Münster, Corrensstrasse 40, 48149 Münster, Germany Ferrocenes in Frustrated Lewis Pair Chemistry M. Mahmun Hossain Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, 3210 N Cramer St, Milwaukee WI 53211, USA The Chemistry of Iron–Alkyl Complexes Laurean Ilies The University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan, 113-0033 Iron-Catalyzed Cross-Coupling Reactions Gerald Kehr Organisch-Chemisches Institut, Universität Münster, Corrensstrasse 40, 48149 Münster, Germany

Ferrocenes in Frustrated Lewis Pair Chemistry Hans-Joachim Knölker Department Chemie, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany The Chemistry of Diene–Iron and Dienyl–Iron Complexes Aleš Korotvička Department of Organic Chemistry, Faculty of Science, Charles University in Prague, Czech Republic. Iron-Mediated Asymmetric Synthesis Martin Kotora Department of Organic Chemistry, Faculty of Science, Charles University in Prague, Czech Republic. Iron-Mediated Asymmetric Synthesis Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, USA, Maryland 21250 The Thermochemistry and Energetics of Organoiron Compounds Diana Liebmann Technische Universität Berlin, Institut für Chemie, Faculty of Science, Str. des 17. Juni 135, 10623, Berlin, Germany Iron Acyl Complexes Hideo Nagashima Institute for Materials Chemistry and Engineering, Kyushu University, Kasuga, Fukuoka 816-8580, Japan Iron-promoted Reduction Reactions Eiichi Nakamura The University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan, 113-0033

Iron-Catalyzed Cross-Coupling Reactions Takashi Nishikata Graduate School of Science and Engineering, Yamaguchi University, Yamaguchi, 755-8611, Japan Iron-promoted Reduction Reactions Sergiu P. Palii University of Florida, Biomedical Mass Spectrometry Laboratory, Clinical Research Center, Gainesville, FL 32610-0322, USA Gas-phase Ion Stereochemistry of Iron Complexes probed by Mass Spectrometric Techniques Karola Rück-Braun Technische Universität Berlin, Institut für Chemie, Faculty of Science, Str. des 17. Juni 135, 10623, Berlin, Germany Iron Acyl Complexes Suzanne W. Slayden George Mason University, 4400 University Drive, Department of Chemistry and Biochemistry, Fairfax, USA, Virginia 22030 The Thermochemistry and Energetics of Organoiron Compounds Petr Štěpnička Faculty of Science, Charles University in Prague, Department of Inorganic Chemistry, Hlavova 2030, Prague, Czech Republic, 12840 The Coordination and Catalytic Chemistry of Phosphinoferrocene Ligands—A Concise Introduction and Update Yusuke Sunada Institute for Materials Chemistry and Engineering, Kyushu University, Kasuga, Fukuoka 816-8580, Japan Iron-promoted Reduction Reactions Joseph S. Ulicki Department of Chemistry and Biochemistry, University of Wisconsin-Milwaukee, 3210 N Cramer St, Milwaukee WI 53211, USA

The Chemistry of Iron–Alkyl Complexes François Volatron Laboratoire de Chimie Théorique, UMR CNRS 7616, UPMC, Sorbonne Universités, 75005 Paris, France Theory of Ferrocenyl Compounds Emmanuel Vrancken Institut Charles Gerhardt UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l&apos;Ecole Normale, 34296 Montpellier Cedex 5, France Organic Transformations Promoted by Lewis Acid Iron Catalysts Naohiko Yoshikai Nanyang Technological University, Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Singapore 637371, Singapore Iron-Catalyzed C&bond;C Bond Formation with C&bond;H Bond Activation Marc Zastrow Technische Universität Berlin, Institut für Chemie, Faculty of Science, Str. des 17. Juni 135, 10623, Berlin, Germany Iron Acyl Complexes

Organogold Compounds (2014)

Alexis Archambeau Laboratoire de Chimie Organique, ESPCI ParisTech, CNRS, 10 rue Vauquelin, 75231 Paris Cedex 05, France. Gold-Catalyzed Reactions of Cyclopropenes Ming Bao State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, PR China. Gold-Catalyzed Benzannulations Hui Chen

Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, PR China. Theory of Gold-Mediated Reactions: From Single Metal Site to Cluster Kai Chen Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, PR China. The Chemistry of Gold–NHC Carbene Complexes Janine Cossy Laboratoire de Chimie Organique, ESPCI ParisTech, CNRS, 10 rue Vauquelin, 75231 Paris Cedex 05, France. Gold-Catalyzed Reactions of Cyclopropenes Chandrakanta Dash Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019-0065, USA. Synthesis and Reactivity of Gold–Olefin Complexes H. V. Rasika Dias Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019-0065, USA. Synthesis and Reactivity of Gold–Olefin Complexes Antonio M. Echavarren Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007 Tarragona, Spain. Gold-Catalyzed Hydroarylation of Alkynes Luis Fernandez Department of Chemistry, University of Zürich, Zürich, CH-8057, Switzerland. Gold-Catalyzed Migrations and Ring Expansions Fabien Gagosz Laboratoire de Synthèse Organique (DCSO), UMR 7652 CNRS, Ecole Polytechnique, 91128 Palaiseau, France.

Gold-Promoted Sigmatropic Rearrangements Yi Gao Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, PR China. Theory of Gold-Mediated Reactions: From Single Metal Site to Cluster Hermenegildo Garcia Instituto de Tecnologia Quimica, CSIC-UPV Universidad Politecnica de Valencia, 46022 Valencia, Spain. Catalysis of Organic Transformations by Gold Nanoparticles Supported on Metal Oxides Emilie Genin Institut des Sciences Moléculaires, UMR 5255, Bâtiment A11, Université de Bordeaux 1, 33405 Talence Cedex, France. Gold-Catalyzed Addition of HX to Alkynes Peng Gu Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, PR China. The Chemistry of Gold–NHC Carbene Complexes A. Stephen K. Hashmi Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany. Gold-Catalyzed and Gold-Mediated Synthesis of Heterocycles Guilhem Henrion Laboratoire de Synthèse Organique (DCSO), UMR 7652 CNRS, Ecole Polytechnique, 91128 Palaiseau, France. Gold-Promoted Sigmatropic Rearrangements César Hurtado-Rodrigo School of Chemistry, University of East Anglia, Norwich NR4 7TJ, UK. The Chemistry of Gold–Allene Complexes Jan S. Jaworski Faculty of Chemistry, University of Warsaw, 02-093 Warszawa, Poland.

Electrochemical Investigations of Organogold Compounds Antonio Laguna Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, 50009 Zaragoza, Spain. The Chemistry of Gold–Metal Bonds Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County (UMBC), Baltimore, MD 21250, USA. Aurocarbons: Binary Gold Carbides, Binary Carbon Aurides and their Derivatives Estibaliz Merino Department of Chemistry, University of Zürich, Zürich, CH-8057, Switzerland. Gold-Catalyzed Migrations and Ring Expansions Christophe Meyer Laboratoire de Chimie Organique, ESPCI ParisTech, CNRS, 10 rue Vauquelin, 75231 Paris Cedex 05, France. Gold-Catalyzed Reactions of Cyclopropenes Veronique Michelet Institut de Recherche de Chimie Paris, UMR CNRS 8247 - Chimie ParisTech, 11 rue P. et M. Curie, 75231, Paris Cedex 05, France. Gold-Catalyzed Addition of HX to Alkynes Frederic Miege Laboratoire de Chimie Organique, ESPCI ParisTech, CNRS, 10 rue Vauquelin, 75231 Paris Cedex 05, France. Gold-Catalyzed Reactions of Cyclopropenes María Paz Muñoz School of Chemistry, University of East Anglia, Norwich NR4 7TJ, UK. The Chemistry of Gold–Allene Complexes Michael E. Muratore Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007 Tarragona, Spain.

Gold-Catalyzed Hydroarylation of Alkynes Cristina Nevado Department of Chemistry, University of Zürich, Zürich, CH-8057, Switzerland. Gold-Catalyzed Migrations and Ring Expansions Richard A. J. O’Hair School of Chemistry, The University of Melbourne, Victoria 3010, Australia; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Victoria 3010, Australia; ARC Centre of Excellence in Free Radical Chemistry and Biotechnology. Mass Spectrometry of Organogold Compounds H. Mark Perks Department of Chemistry and Biochemistry, University of Maryland, Baltimore County (UMBC), Baltimore, MD 21250, USA. Aurocarbons: Binary Gold Carbides, Binary Carbon Aurides and their Derivatives Min Shi Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, PR China; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, PR China. The Chemistry of Gold–NHC Carbene Complexes Cristian Silvestru Faculty of Chemistry & Chemical Engineering, Chemistry Department, Babes-Bolyai University, RO-400028 Cluj-Napoca, Romania. The Chemistry of Gold–Metal Bonds Manolis Stratakis Department of Chemistry, University of Crete, 71003 Voutes, Iraklion, Greece. Catalysis of Organic Transformations by Gold Nanoparticles Supported on Metal Oxides Balaram S. Takale State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, PR China.

Gold-Catalyzed Benzannulations F. Dean Toste Department of Chemistry, University of California, 419 Latimer Hall, Berkeley, CA 94720-1460, USA. The Chemistry of Gold fluoride Complexes Mie Højer Vilhelmsen Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany. Gold-Catalyzed and Gold-Mediated Synthesis of Heterocycles J. Mathias Weber JILA and Department of Chemistry and Biochemistry, 440 UCB, University of Colorado, Boulder, CO 80309-0440, USA. Gas Phase Chemistry of Gold William J. Wolf Department of Chemistry, University of California, 419 Latimer Hall, Berkeley, CA 94720-1460, USA. The Chemistry of Gold fluoride Complexes Yoshinori Yamamoto State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, PR China; WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan. Gold-Catalyzed Benzannulations Jun Zhang Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, PR China. The Chemistry of Gold–NHC Carbene Complexes

Peroxides (2014)

Alexandru T. Balaban Department of Marine Sciences, University of Texas at Galveston, Galveston, TX 77553-1675, USA. An Introduction to the Consequences of Spin and Bond Strength in the Chemistry of Diatomic Oxygen, Peroxides, and Related Species Stephen J. Blanksby Central Analytical Research Facility, Institute for Future Environments, Queensland University of Technology, Brisbane, Queensland 4000, Australia. Gas-Phase Ion Chemistry of Organic Peroxides Jean Cadet Institut Nanosciences et Cryogénie, Direction des Sciences de la Matière, CEA/Grenoble, F-38054 Grenoble Cedex 9, France. [18O]-Peroxides: Synthesis and Biological Applications Ekaterina M. Chainikova Institute of Organic Chemistry, Ufa Scientific Centre, Russian Academy of Sciences, Ufa, Bashkortostan 450054, Russia. The chemistry of nitroso oxides Edward L. Clennan Department of Chemistry, University of Wyoming, Laramie, WY 82071, USA. 1,2-Dioxatrisulfane (thiaperoxide) intermediates in type I and II photooxygenation reactions Patrick H. Dussault Department of Chemistry, University of Nebraska–Lincoln, Lincoln, NE 68588-0304, USA. 1,1-Dihydroperoxides Werner Fudickar Department of Chemistry, University of Potsdam, Karl-Liebknecht-Str. 24-25, D-14476 Potsdam, Germany. Applications of Endoperoxides derived from Acenes and Singlet Oxygen Isaac Garcia-Bosch Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA.

Copper Peroxide Bioinorganic Chemistry: From Metalloenzymes to Bioinspired Synthetic Systems Albert W. Girotti Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226-0509, USA. Generation and Reactivity of Lipid Hydroperoxides in Biological Systems María Elena González Núñez Departamento de Química Orgánica, Universidad de Valencia, E-46100 Valencia, Spain. Reactions of Peroxides on Solid Surfaces Alexander Greer Department of Chemistry, The City University of New York, Brooklyn College, Brooklyn, NY 11210, USA. An Introduction to the Consequences of Spin and Bond Strength in the Chemistry of Diatomic Oxygen, Peroxides, and Related Species Kenneth D. Karlin Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. Copper Peroxide Bioinorganic Chemistry: From Metalloenzymes to Bioinspired Synthetic Systems Shuji Kato Department of Chemistry, School of Medicine, Toho University, Ota-ku, Tokyo 143-8540, Japan. Gas-Phase ion Chemistry of Organic Peroxides Sergey L. Khursan Institute of Organic Chemistry, Ufa Scientific Centre, Russian Academy of Sciences, Ufa, Bashkortostan 450054, Russia. Organic tetroxides and mechanism of peroxy radical recombination The chemistry of nitroso oxides Peroxide intermediates of oxidation processes: Organic trioxides

Thomas M. Klapötke Department of Chemistry, Energetic Materials Research, Ludwig-Maximilian University Munich (LMU), 81377 Munich, Germany. Peroxide Explosives Witold Korytowski Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226-0509, USA; Department of Biophysics, Jagiellonian University, Krakow, Poland. Generation and Reactivity of Lipid Hydroperoxides in Biological Systems Keith T. Kuwata Department of Chemistry, Macalester College, Saint Paul, MN 55105, USA. Computational Treatments of Peroxy Radicals in Combustion and Atmospheric Reactions Quantum chemical studies of carbonyl oxide chemistry in combustion and in the lower atmosphere Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County (UMBC), Baltimore, MD 21250, USA. An Introduction to the Consequences of Spin and Bond Strength in the Chemistry of Diatomic Oxygen, Peroxides, and Related Species Torsten Linker Department of Chemistry, University of Potsdam, Karl-Liebknecht-Str. 24-25, D-14476 Potsdam, Germany. Applications of Endoperoxides derived from Acenes and Singlet Oxygen Tetsuro Majima The Institute of Scientific and Industrial Research (SANKEN), Osaka University, Ibaraki, Osaka 567-0047, Japan. Single-Molecule Reactive Oxygen Species Detection in Photocatalytic Reactions Sergei V. Makarov

Department of Food Chemistry and Biotechnology, State University of Chemistry and Technology, Ivanovo 153000, Russia. Sulfoxylic and Thiosulfurous Acids and their Dialkoxy Derivatives Anna S. Makarova G.A. Krestov Institute of Solution Chemistry of RAS, Ivanovo 153045, Russia. Sulfoxylic and Thiosulfurous Acids and their Dialkoxy Derivatives Glaucia R. Martinez Departamento de Bioquímica e Biologia Molecular, Centro Politécnico, Setor de Ciências Biológicas, Universidade Federal do Paraná, CP 19046, CEP 81531-990, Jd das Américas, Curitiba, PR, Brazil. [18O]-Peroxides: Synthesis and Biological Applications Paolo Di Mascio Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CP 26077, CEP 05508-000, São Paulo, SP, Brazil. [18O]-Peroxides: Synthesis and Biological Applications Gerald McDonnell STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, USA. The Use of Hydrogen Peroxide for Disinfection and Sterilization Applications Marisa H. G. Medeiros Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CP 26077, CEP 05508-000, São Paulo, SP, Brazil. [18O]-Peroxides: Synthesis and Biological Applications Rossella Mello Departamento de Química Orgánica, Universidad de Valencia, E-46100 Valencia, Spain. Reactions of Peroxides on Solid Surfaces Sayuri Miyamoto Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CP 26077, CEP 05508-000, São Paulo, SP, Brazil. [18O]-Peroxides: Synthesis and Biological Applications Gregory Nkepang

Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73117, USA; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019, USA. Heteroatom-substitued Dioxetanes and their Emerging Biomedical Applications Rustam L. Safiullin Institute of Organic Chemistry, Ufa Scientific Centre, Russian Academy of Sciences, Ufa, Bashkortostan 450054, Russia. The chemistry of nitroso oxides Chris Schwartz Department of Chemistry, University of Nebraska–Lincoln, Lincoln, NE 68588-0304, USA. 1,1-Dihydroperoxides Matthias Selke Department of Chemistry and Biochemistry, California State University, Los Angeles, Los Angeles, CA 90032, USA. Reactions of Metal Complexes with Singlet Oxygen Radu Silaghi-Dumitrescu Department of Chemistry, Babes-Bolyai University, Cluj-Napoca RO-400028, Romania. Sulfoxylic and Thiosulfurous Acids and their Dialkoxy Derivatives Takashi Tachikawa The Institute of Scientific and Industrial Research (SANKEN), Osaka University, Ibaraki, Osaka 567-0047, Japan. Single-Molecule Reactive Oxygen Species Detection in Photocatalytic Reactions Thomas Wloka Department of Chemistry, Energetic Materials Research, Ludwig-Maximilian University Munich (LMU), 81377 Munich, Germany. Peroxide Explosives Youngjae You Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73117, USA; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019, USA. Heteroatom-substitued Dioxetanes and their Emerging Biomedical Applications

Metal Enolates (2016)

David Adner Faculty of Natural Sciences, Institute of Chemistry, Inorganic Chemistry, Technische Universität Chemnitz, 09107, Chemnitz, Germany Advances in Deposition of Main-Group Metal Oxides and Rare-Earth Oxides from Metal Enolates Advances in Deposition of Metals from Metal Enolates Advances in Deposition of Transition-Metal Oxides from Metal Enolates Meiko Arisawa Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Sendai 980–8578, Japan Rhodium Enolate Complexes as Synthons and Catalysts in Organic Chemistry Erick L. Bastos Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, Brazil Acid–Base and Solvation properties of Metal Enolates. Part 1: The Enolate Ion and Main-Group Metal Enolates Acid–Base and Solvation properties of Metal Enolates. Part 2: Transition-Metal Enolates and Medium Effects Paola Deplano Dipartimento di Fisica, Università di Cagliari, S.S. 554-Bivio per Sestu, I09042, Monserrato-Cagliari, Italy Recent Advances in the Structure and Properties of Metal–Dithiolene Complexes Davide Espa Dipartimento di Scienze Chimiche e Geologiche, Università di Cagliari, S.S. 554-Bivio per Sestu, I09042, Monserrato–Cagliari, Italy Recent Advances in the Structure and Properties of Metal–Dithiolene Complexes

Colin Georgi Faculty of Electrical Engineering and Information Technology, Microtechnology, Center for Microtechnology, Technische Universität Chemnitz, 09107, Chemnitz, Germany Advances in Deposition of Main-Group Metal Oxides and Rare-Earth Oxides from Metal Enolates Advances in Deposition of Metals from Metal Enolates Advances in Deposition of Transition-Metal Oxides from Metal Enolates Christine Jérôme Center for Education and Research on Macromolecules (CERM), Chemistry Department, University of Liège, B-4000 Liège, Belgium Enolates in Macromolecular Science: Current Situation and Future Outlook Katerina M. Korch Department of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA Asymmetric Synthesis of Quaternary Stereocenters via Metal Enolates Heinrich Lang Faculty of Natural Sciences, Institute of Chemistry, Inorganic Chemistry, Technische Universität Chemnitz, 09107, Chemnitz, Germany Advances in Deposition of Main-Group Metal Oxides and Rare-Earth Oxides from Metal Enolates Advances in Deposition of Metals from Metal Enolates Advances in Deposition of Transition-Metal Oxides from Metal Enolates

Philippe Lecomte Center for Education and Research on Macromolecules (CERM), Chemistry Department, University of Liège, B-4000 Liège, Belgium Enolates in Macromolecular Science: Current Situation and Future Outlook Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA

Aspects of the Energetics of Metal β- Diketonates and their Derivatives Steven A. Loskot Department of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA Asymmetric Synthesis of Quaternary Stereocenters via Metal Enolates Kenji Matsumoto Department of Fundamental Organic Chemistry, Institute for Materials Chemistry and Engineering, Kyushu University, Kasuga-koen, Kasuga, 816-8580, Japan Recent Advances in the Chemistry of Metal Ynolates William R. Patton Department of Chemistry, Bates College, Lewiston, ME 04240, USA

Advances in the use of Lanthanide Enolates as Nuclear Magnetic Resonance Shift Reagents Luca Pilia Dipartimento di Ingegneria Meccanica, Chimica e dei Materiali, Università di Cagliari, Via Marengo 2, I09123, Cagliari, Italy Recent Advances in the Structure and Properties of Metal–Dithiolene Complexes Maja Ponikvar-Svet Department of Inorganic Chemistry and Technology, Jožef Stefan Institute, SI-1000 Ljubljana, Slovenia Aspects of the Energetics of Metal β- Diketonates and their Derivatives Mitsuru Shindo Department of Fundamental Organic Chemistry, Institute for Materials Chemistry and Engineering, Kyushu University, Kasuga-koen, Kasuga, 816-8580, Japan Recent Advances in the Chemistry of Metal Ynolates Brian M. Stoltz Department of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA Asymmetric Synthesis of Quaternary Stereocenters via Metal Enolates

Thomas J. Wenzel Department of Chemistry, Bates College, Lewiston, ME 04240, USA

Advances in the use of Lanthanide Enolates as Nuclear Magnetic Resonance Shift Reagents Masahiko Yamaguchi Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Sendai 980–8578, Japan Rhodium Enolate Complexes as Synthons and Catalysts in Organic Chemistry Jacob Zabicky Department of Chemical Engineering, Ben-Gurion University of the Negev, Beer-Sheva, 84105, Israel Recent Advances in Electrochemical Analytical Methods Involving Metal Enolates Recent Advances in Nonelectrochemical Analytical Methods Involving Metal Enolates Diana N. Zeiger Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA Aspects of the Energetics of Metal β- Diketonates and their Derivatives

Metal Phenolates (2016)

Shigehisa Akine Graduate School of Natural Science and Technology,Kanazawa University, Kanazawa 920-1192, Japan Metal Complexes with Oligo(Salen)-Type Ligands Erick L. Bastos Department of Fundamental Chemistry, University of São Paulo, 05508-000 São Paulo, SP, Brazil Recent Advances in Acid-Base and Solvation Properties of Metal Phenolates Hermi F. Brito Department of Fundamental Chemistry, University of São Paulo, 05508-000 São Paulo, SP, Brazil

Photophysical and Structural Properties of Rare-Earth Phenolate Compounds Renzo Cini Former Professor of Inorganic Chemistry, University of Siena, Siena, Italy Recent Advances in Biomimetic Metal Phenolates Peter J. Cragg School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton BN2 4GJ, UK Coordination Chemistry and Applications of Phenolic Homooxa- and Homoazacalixarene-Metal Complexes Coordination Chemistry and Applications of Phenolic Thiacalixarene-Metal Complexes Samuel Dagorne Department of Chemistry, SRCO Group, Institute of Chemistry, University of Strasbourg-CNRS, 67000 Strasbourg, France Polymerization Catalysis by Metal Phenolates Maria Claudia F. C. Felinto Institute of Nuclear Energy and Research, Av. Prof Lineu Prestes 2242 Cidade Universitária, 05508-000 São Paulo, SP, Brazil Photophysical and Structural Properties of Rare-Earth Phenolate Compounds Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA Contemporary Use of Azophenolates and Related Species in the Determination of Metal Cations Caroline O. Machado Department of Fundamental Chemistry, University of São Paulo, 05508-000 São Paulo, SP, Brazil Recent Advances in Acid-Base and Solvation Properties of Metal Phenolates Oscar M. L. Malta

Department of Chemistry, Federal University of Paraiba, Cidade Universitária, João Pessoa-PB 58051-970, Brazil; Department of Fundamental Chemistry, Federal University of Pernambuco, CCEN Cidade Universitária, Recife-PE, 50670-901, Brazil Photophysical and Structural Properties of Rare-Earth Phenolate Compounds Paula M. Marcos Faculty of Pharmacy, University of Lisbon, 1649-003, Lisbon, Portugal; Center of Structural Chemistry (CQE), Faculty of Sciences, University of Lisbon, 1749-016, Lisbon, Portugal Coordination Chemistry and Applications of Phenolic Homooxa- and Homoazacalixarene-Metal Complexes Coordination Chemistry and Applications of Phenolic Thiacalixarene-Metal Complexes Dina M. B. Murtinho Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra, Portugal Advances in the Catalysis of Organic Processes by Metal Phenolates Maja Ponikvar-Svet Department of Inorganic Chemistry and Technology, Jožef Stefan Institute, SI-1000 Ljubljana, Slovenia Contemporary Use of Azophenolates and Related Species in the Determination of Metal Cations Lucas C. V. Rodrigues Department of Fundamental Chemistry, University of São Paulo, 05508-000 São Paulo, SP, Brazil Photophysical and Structural Properties of Rare-Earth Phenolate Compounds Charles Romain Department of Chemistry, Imperial College London, South Kensington Campus, London SW7 2AZ, UK Polymerization Catalysis by Metal Phenolates Yuichi Shimazaki College of Science, Ibaraki University, Bunkyo, Mito 310-8512, Japan

Recent Advances in the Field of Phenoxyl Radical-Metal Complexes Maria Elisa da Silva Serra Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra, Portugal Advances in the Catalysis of Organic Processes by Metal Phenolates Gabriella Tamasi Department of Biotechnology, Chemistry and Pharmacy, University of Siena, I-53100 Siena, Italy; Center for Colloid and Surface Science (CSGI), I-50019 Sesto Fiorentino, Italy Recent Advances in Biomimetic Metal Phenolates Ercules E. S. Teotonio Department of Chemistry, Federal University of Paraiba, Cidade Universitária, João Pessoa-PB, 58051-970, Brazil Photophysical and Structural Properties of Rare-Earth Phenolate Compounds Jacob Zabicky Department of Chemical Engineering, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel Advances in the Analytical Chemistry of Metal Phenolates

Organoaluminum Compounds (2016)

Carla C. P. Arruda Centro de Ciências Biológicas e da Saúde, Universidade Federal do Mato Grosso do Sul, Campo Grande, MS, CEP 79070-900, Brazil Hydroalumination of Alkenes and Alkynes Doron Aurbach Department of Chemistry, Bar-Ilan University, Ramat-Gan 5290002, Israel Electrochemistry of Organoaluminum Compounds Adriano C. M. Baroni Centro de Ciências Biológicas e da Saúde, Universidade Federal do Mato Grosso do Sul, Campo Grande, MS, CEP 79070-900, Brazil

Hydroalumination of Alkenes and Alkynes Ghenwa Bouhadir UPS, Laboratoire Hétérochimie Fondamentale Appliquée, UMR 5069 CNRS-UPS Université de Toulouse, F-31062 Toulouse, France Organoaluminum Compounds and Lewis Pairs Didier Bourissou UPS, Laboratoire Hétérochimie Fondamentale Appliquée, UMR 5069 CNRS-UPS Université de Toulouse, F-31062 Toulouse, France Organoaluminum Compounds and Lewis Pairs Diego B. Carvalho Centro de Ciências Biológicas e da Saúde, Universidade Federal do Mato Grosso do Sul, Campo Grande, MS, CEP 79070-900, Brazil Hydroalumination of Alkenes and Alkynes Scott Collins Department of Chemistry, University of Victoria, Victoria, BC V8W 3V6, Canada Mass Spectrometry of Organoaluminum Derivatives Odile Eisenstein Institut Charles Gerhardt, CNRS UMR 5253, Université de Montpellier,34095 Montpellier, France and Centre for Theoretical and Computational Chemistry (CTCC), Department of Chemistry, University of Oslo, N-0315 Oslo, Norway Structure, Bonding, and Reactivity of Organoaluminum Molecular Species: A Computational Perspective Hélène Gérard Sorbonne Universités, UPMC Univ Paris 06, CNRS, Laboratoire de Chimie Théorique, UMR 7616, F-75005 Paris, France Structure, Bonding, and Reactivity of Organoaluminum Molecular Species: A Computational Perspective Yosef Gofer Department of Chemistry, Bar-Ilan University, Ramat-Gan 5290002, Israel Electrochemistry of Organoaluminum Compounds

Mohamed Haouas Tectospin Group, Institut Lavoisier de Versailles (UMR CNRS 8180), Université de Versailles Saint Quentin en Yvelines, 78035 Versailles, France The Use of 27Al NMR to Study Aluminum Compounds: A Survey of the Last 25 Years Amir H. Hoveyda Department of Chemistry, Merkert Chemistry Center, Chestnut Hill, MA 02467, USA Organoaluminum Compounds in Catalytic Enantioselective C–C Bond Forming Reactions Shouquan Huo Department of Chemistry, East Carolina University, Greenville, NC 27858, USA Carboalumination Reactions Olivier Jackowski Institut Parisien de Chimie Moléculaire, IPCM, UMR 8232 CNRS, UPMC Sorbonne Universités, 75252 Paris Cedex 05, France The Chemistry of Alkynyaluminum Species Paul Knochel Chemistry Department, Ludwig-Maximilians University Munich, D-81377, Munich, Germany The Preparation and Cross-Coupling Reactions of Organoaluminum Compounds Marcus Layh Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, 48149 Münster, Germany Organoaluminum Compounds and Lewis Pairs Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County (UMBC), Baltimore, MD 21250, USA Aspects of the Chemical Energetics of Carbon–Aluminum Bonded Species Vladimir Malakhov Chemistry Department, Ludwig-Maximilians University Munich, D-81377, Munich, Germany

The Preparation and Cross-Coupling Reactions of Organoaluminum Compounds Charlotte Martineau Tectospin Group, Institut Lavoisier de Versailles (UMR CNRS 8180), Université de Versailles Saint Quentin en Yvelines, 78035 Versailles, France The Use of 27Al NMR to Study Aluminum Compounds: A Survey of the Last 25 Years Seijiro Matsubara Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo, Kyoto, 606-8501, Japan The Chemistry of Bis-Aluminated Compounds Kevin P. McGrath Department of Chemistry, Merkert Chemistry Center, Chestnut Hill, MA 02467, USA Organoaluminum Compounds in Catalytic Enantioselective C–C Bond Forming Reactions J. Scott McIndoe Department of Chemistry, University of Victoria, Victoria, BC V8W 3V6, Canada Mass Spectrometry of Organoaluminum Derivatives Laurent Micouin Laboratoire de Chimie et de Biochimie pharmacologiques et toxicologiques, LCBPT, UMR 8601 CNRS, Université Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France The Chemistry of Alkynyaluminum Species Riccardo Piccardi Laboratoire de Chimie et de Biochimie pharmacologiques et toxicologiques, LCBPT, UMR 8601 CNRS, Université Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France The Chemistry of Alkynyaluminum Species Michael Salama Department of Chemistry, Bar-Ilan University, Ramat-Gan 5290002, Israel Electrochemistry of Organoaluminum Compounds Ivgeni Shterenberg Department of Chemistry, Bar-Ilan University, Ramat-Gan 5290002, Israel

Electrochemistry of Organoaluminum Compounds Suzanne W. Slayden Department of Chemistry and Biochemistry, George Mason University, Fairfax, VA 22030, USA Aspects of the Chemical Energetics of Carbon–Aluminum Bonded Species Rhonda L. Stoddard Department of Chemistry, University of Victoria, Victoria, BC V8W 3V6, Canada Mass Spectrometry of Organoaluminum Derivatives Francis Taulelle Tectospin Group, Institut Lavoisier de Versailles (UMR CNRS 8180), Université de Versailles Saint Quentin en Yvelines, 78035 Versailles, France The Use of 27Al NMR to Study Aluminum Compounds: A Survey of the Last 25 Years Werner Uhl Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, 48149 Münster, Germany Organoaluminum Compounds and Lewis Pairs Rudolf J. Wehmschulte Department of Chemistry, Florida Institute of Technology, Melbourne, FL 32901, USA The Chemistry of Low-Valent Organoaluminum Species

Nitrogen-rich Functional Groups (2017) Alexandru T. Balaban Department of Marine Sciences, Texas A&M University at Galveston, Galveston, TX 77553-1675, USA Stable Hydrazyls and Push-Pull (Capto-Dative) Aminyl Free Radicals Klaus Banert Organic Chemistry, Chemnitz University of Technology, 09111 Chemnitz, Germany New Combinations of Organic Azides and Adjacent Functional Groups

Yuan Chen Chemistry Department, Rutgers, The State University of New Jersey, Newark, NJ 07102, USA Click Chemistry and Nitrogen-Containing Heterocycles Formed in Surface Functionalization Reactions Hao Fan Chemistry Department, Rutgers, The State University of New Jersey, Newark, NJ 07102, USA Click Chemistry and Nitrogen-Containing Heterocycles Formed in Surface Functionalization Reactions Vera L. S. Freitas CIQ_UP, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal Thermochemical Insights on Small Nitrogen Heterocyclic Compounds Elena Galoppini Chemistry Department, Rutgers, The State University of New Jersey, Newark, NJ 07102, USA Click Chemistry and Nitrogen-Containing Heterocycles Formed in Surface Functionalization Reactions Jane S. Murray Department of Chemistry, University of New Orleans, New Orleans, 70148 LA, USA N-Oxides of Polyazoles and Polyazines Nitrogen Catenation: Polyazoles and Polyazines Peter Politzer Department of Chemistry, University of New Orleans, New Orleans, 70148 LA, USA

N-Oxides of Polyazoles and Polyazines Nitrogen Catenation: Polyazoles and Polyazines

Maria D. M. C. Ribeiro da Silva CIQ_UP, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal

Thermochemical Insights on Small Nitrogen Heterocyclic Compounds

Hypervalent Halogen Compounds (2018) Andrey P. Antonchick Department of Chemical Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany Department of Chemistry and Chemical Biology, Technical University of Dortmund, 44221 Dortmund, Germany Faculty of Science, Peoples’ Friendship University of Russia, 117198 Moscow, Russia Oxidative Heteroatom-Heteroatom Bond Formation Luis Bering Department of Chemical Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany Department of Chemistry and Chemical Biology, Technical University of Dortmund, 44221 Dortmund, Germany Oxidative Heteroatom-Heteroatom Bond Formation Timo Broese Institute of Chemistry, Rostock University, 18059 Rostock, Germany Electrochemistry of Hypervalent Iodine Compounds Sylvain Canesi Laboratoire de Méthodologie et Synthèse de Produits Naturels, University of Quebec at Montreal, Montreal, H3C 3P8, Quebec, Canada Rearrangements and Fragmentations Mediated by Hypervalent Iodine Reagents Yiyun Chen State Key Laboratory of Bioorganic and Natural Products Chemistry, Centre of Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, PR China Photochemistry of Hypervalent Iodine Compounds Toshifumi Dohi

Department of Pharmaceutical Sciences, Ritsumeikan University, Shiga 525-8577, Japan Oxidative C–C Bond Formation (Couplings, Cyclizations, Cyclopropanation, etc.) Robert Francke Institute of Chemistry, Rostock University, 18059 Rostock, Germany Electrochemistry of Hypervalent Iodine Compounds Zsombor Gonda ELTE “Lendület” Catalysis and Organic Synthesis Research Group, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary, H-1117 Transition Metal-Catalyzed Reactions with Iodine(III) Reagents Durga Prasad Hari Laboratory of Catalysis and Organic Synthesis, Swiss Federal Institute of Technology in Lausanne, EPFL SB ISIC LCSO, 1015 Lausanne, Switzerland Alkynylations and Vinylations Kazuaki Ishihara Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Chikusa 464-8603, Japan Oxidation of Alcohols and Amines Benson Jelier Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Halogenation and Perfluoroalkylation Chemistry Using Hypervalent Halogen Compounds Kunfang Jia State Key Laboratory of Bioorganic and Natural Products Chemistry, Centre of Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, PR China Photochemistry of Hypervalent Iodine Compounds Michael W. Justik Department of Chemistry, Penn State Behrend, Erie, PA 16563-0203, USA Structural Chemistry of Hypervalent Iodine Compounds

Tatsuo Kaiho Godo Shigen Co., Ltd., Tokyo, Japan Industrial Applications Dmitry Katayev Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Halogenation and Perfluoroalkylation Chemistry Using Hypervalent Halogen Compounds Yasuyuki Kita Research Center for Drug Discovery and Pharmaceutical Development Science, Ritsumeikan University, Shiga 525-8577, Japan Oxidative C–C Bond Formation (Couplings, Cyclizations, Cyclopropanation, etc.) Joel F. Liebman Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD 21250, USA Aspects of the Chemical Energetics of the Hypervalent Benzene-Based Organohalogen Halosyl, Halyl, and Perhalyl Species Shuiyu Lu Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA Hypervalent Iodine Compounds as Precursors for Biomedical Radiotracers Hans Peter Lüthi Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Fundamental Aspects of Structure, Bonding, and the Reactivity of Hypervalent Iodine Compounds Halua Pinto de Magalhães Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Fundamental Aspects of Structure, Bonding, and the Reactivity of Hypervalent Iodine Compounds

Kazunori Miyamoto Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan Chemistry of Hypervalent Bromine Kilian Muñiz Institute of Chemical Research of Catalonia (ICIQ), 43007 Tarragona, Spain; Catalan Institution for Research and Advanced Studies (ICREA), 08010 Barcelona, Spain Carbon-Heteroatom Bond Formation Mediated by Hypervalent Iodine Stefano Nicolai Laboratory of Catalysis and Organic Synthesis, Swiss Federal Institute of Technology in Lausanne, EPFL SB ISIC LCSO, 1015 Lausanne, Switzerland Alkynylations and Vinylations Zoltán Novák ELTE “Lendület” Catalysis and Organic Synthesis Research Group, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary, H-1117 Transition Metal-Catalyzed Reactions with Iodine(III) Reagents Richard A. J. O’Hair School of Chemistry, The University of Melbourne, Victoria 3010, Australia; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Victoria 3010, Australia Mass Spectrometry and Gas-Phase Ion Chemistry of Hypervalent Halogen Compounds Berit Olofsson Department of Organic Chemistry, Stockholm University, 106 91 Stockholm, Sweden Arylations Promoted by Hypervalent Iodine Reagents Victor W. Pike Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA Hypervalent Iodine Compounds as Precursors for Biomedical Radiotracers Maja Ponikvar-Svet

Department of Inorganic Chemistry and Technology, Jožef Stefan Institute, SI-1000 Ljubljana, Slovenia Aspects of the Chemical Energetics of the Hypervalent Benzene-Based Organohalogen Halosyl, Halyl, and Perhalyl Species Arend F. Roesel Institute of Chemistry, Rostock University, 18059 Rostock, Germany Electrochemistry of Hypervalent Iodine Compounds R. Martin Romero Institute of Chemical Research of Catalonia (ICIQ), 43007 Tarragona, Spain Carbon-Heteroatom Bond Formation Mediated by Hypervalent Iodine Oliver Sala Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Fundamental Aspects of Structure, Bonding, and the Reactivity of Hypervalent Iodine Compounds Alexandr Shafir Institute of Chemical Research of Catalonia (ICIQ), Barcelona Institute of Science and Technology, 43007 Tarragona, Spain NMR of Hypervalent Iodine Compounds Fabrice G. Siméon Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA Hypervalent Iodine Compounds as Precursors for Biomedical Radiotracers Fateh V. Singh Chennai Campus, VIT University, Chennai 600127, Tamil Nadu, India Stereoselective Reactions Sanjay Telu Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA

Hypervalent Iodine Compounds as Precursors for Biomedical Radiotracers Antonio Togni Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology in Zurich (ETH Zürich), 8093 Zürich, Switzerland Halogenation and Perfluoroalkylation Chemistry Using Hypervalent Halogen Compounds Gergely L. Tolnai ELTE “Lendület” Catalysis and Organic Synthesis Research Group, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary, H-1117 Transition Metal-Catalyzed Reactions with Iodine(III) Reagents Muhammet Uyanik Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Chikusa 464-8603, Japan Oxidation of Alcohols and Amines Piret Villo Department of Organic Chemistry, Stockholm University, 106 91 Stockholm, Sweden Arylations Promoted by Hypervalent Iodine Reagents Jerome Waser Laboratory of Catalysis and Organic Synthesis, Swiss Federal Institute of Technology in Lausanne, EPFL SB ISIC LCSO, 1015 Lausanne, Switzerland Alkynylations and Vinylations Sarah E. Wengryniuk Department of Chemistry, Temple University, Philadelphia, PA 19122, USA Rearrangements and Fragmentations Mediated by Hypervalent Iodine Reagents Thomas Wirth School of Chemistry, Cardiff University, Cardiff, CF10 3AT, UK Stereoselective Reactions Yichen Wu

Institute of Chemical Research of Catalonia (ICIQ), Barcelona Institute of Science and Technology, 43007 Tarragona, Spain NMR of Hypervalent Iodine Compounds Viktor V. Zhdankin Department of Chemistry and Biochemistry, University of Minnesota Duluth, Duluth, MN 55812, USA Industrial Applications Synthesis of Hypervalent Iodine Compounds for Oxidation Reactions