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Catalytic and enantioselective allylic C-H activation with donor-acceptor-substituted carbenoids.

作者信息

Davies Huw M L, Nikolai Joachim

机构信息

Department of Chemistry, University at Buffalo, The State University of New York, Buffalo 14260, USA.

出版信息

Org Biomol Chem. 2005 Dec 7;3(23):4176-87. doi: 10.1039/b509425a. Epub 2005 Oct 31.

DOI:10.1039/b509425a
PMID:16294245
Abstract

In this perspective we give an overview of enantioselective C-H activation at allylic sites by means of rhodium(II)-stabilized donor-acceptor-substituted carbenoids. This methodology has been proven to be both an equivalent to established asymmetric reaction sequences and a new synthetic approach with no established counterpart in organic synthesis.

摘要

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