cheminform abstract: iron oligopyridine complexes as efficient catalysts for practical oxidation of...
TRANSCRIPT
OxidationO 0212 DOI: 10.1002/chin.201209035
Iron Oligopyridine Complexes as Efficient Catalysts for Practical Oxidation of Arenes, Alkanes, Tertiary Amines and N-Acyl Cyclic Amines with Oxone. — A cationic Fe—quinquepyridine complex is successfully applied to the Oxone-mediated epoxidation of alkenes, e.g. (I), (III) and (VI), the oxidation of arenes to quinones[cf. (VIII), (X)], the demethylation of tertiary N-methylamines (XX), the oxidative ring opening of cyclic N-acylamines [cf. (XXVI)] as well as to the α-cyanation of amines [cf. (XXa), (XXIV)]. The loss of iron in the complex can be compensated by addition of Fe(ClO4)2. Use of SBA-15-immobilized terpyridine as ligand allows for easy recov-ery of the ligand, although the loss of iron is still observed. — (LIU, P.; LIU, Y.; WONG, E. L.-M.; XIANG, S.; CHE*, C.-M.; Chem. Sci. 2 (2011) 11, 2187-2195, http://dx.doi.org/10.1039/c1sc00234a ; Dep. Chem., Univ. Hong Kong, Kowloon, Hong Kong, Peop. Rep. China; Eng.) — Mischke
09- 035
ChemInform 2012, 43, issue 09 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
ChemInform 2012, 43, issue 09 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim