cheminform abstract: synthesis and chemical reactivity of new azaenamines incorporated the...

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ChemInform 2010, 41, issue 31 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Benzothiophene derivatives R 0100 DOI: 10.1002/chin.201031111 Synthesis and Chemical Reactivity of New Azaenamines Incorporated the 4,5,6,7-Tetrahydrobenzo[b]thiophene Moiety: [3 + 3] Atom Combination. A new, simple and efficient route to azaenamines incorporating a tetrahydrobenzothio- phene moiety is developed. The azaenamines (III) are shown to be valuable precursors for the synthesis of fused pyridazine derivatives via [3 + 3] atom combination reac- tions. — (ABDELHAMID*, I. A.; DARWISH, E. S.; NASRA, M. A.; ABDEL-GALLIL, F. M.; FLEITA, D. H.; Synthesis 2010, 7, 1107-1112, DOI:10.1055/s-0029-1219235; Dep. Chem., Fac. Sci., Cairo Univ., Giza 12613, Egypt; Eng.) — Mais 31- 111

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www.cheminform.wiley-vch.de

Benzothiophene derivativesR 0100 DOI: 10.1002/chin.201031111

Synthesis and Chemical Reactivity of New Azaenamines Incorporated the 4,5,6,7-Tetrahydrobenzo[b]thiophene Moiety: [3 + 3] Atom Combination. — A new, simple and efficient route to azaenamines incorporating a tetrahydrobenzothio-phene moiety is developed. The azaenamines (III) are shown to be valuable precursors for the synthesis of fused pyridazine derivatives via [3 + 3] atom combination reac-tions. — (ABDELHAMID*, I. A.; DARWISH, E. S.; NASRA, M. A.; ABDEL-GALLIL, F. M.; FLEITA, D. H.; Synthesis 2010, 7, 1107-1112, DOI:10.1055/s-0029-1219235; Dep. Chem., Fac. Sci., Cairo Univ., Giza 12613, Egypt; Eng.) — Mais

31- 111

ChemInform 2010, 41, issue 31 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim