cheminform abstract: cyclopropylation of arylamines at the 2-position with cyclopropylmagnesium...

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ChemInform 2010, 41, issue 10 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Amines Q 0120 DOI: 10.1002/chin.201010066 Cyclopropylation of Arylamines at the 2-Position with Cyclopropylmagnesium Carbenoids. — The process for the cyclopropylation of C-atoms requires at least one methyl substituent on the cyclopropane ring. The reaction with meta-substituted ani- lines proceeds with moderate regioselectivity (to be continued). — (YAMADA, Y.; MIZUNO, M.; NAGAMOTO, S.; SATOH*, T.; Tetrahedron 65 (2009) 48, 10025-10030; Grad. Sch. Chem. Sci. Technol., Sci. Univ. Tokyo, Shinjuku, Tokyo 162, Japan; Eng.) — Y. Steudel 10- 066

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www.cheminform.wiley-vch.de

AminesQ 0120 DOI: 10.1002/chin.201010066

Cyclopropylation of Arylamines at the 2-Position with Cyclopropylmagnesium Carbenoids. — The process for the cyclopropylation of C-atoms requires at least one methyl substituent on the cyclopropane ring. The reaction with meta-substituted ani-lines proceeds with moderate regioselectivity (to be continued). — (YAMADA, Y.; MIZUNO, M.; NAGAMOTO, S.; SATOH*, T.; Tetrahedron 65 (2009) 48, 10025-10030; Grad. Sch. Chem. Sci. Technol., Sci. Univ. Tokyo, Shinjuku, Tokyo 162, Japan; Eng.) — Y. Steudel

10- 066

ChemInform 2010, 41, issue 10 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim