Catalytic Enantioselective Reformatsky Reaction with ortho-Substituted Diarylketones

Abstract

The catalytic enantioselective Reformatsky reaction with ortho-substituted diarylketones with good enantioselectivities and moderate to good yields is reported. A readily available BINOL derivative is used as a chiral catalyst, and the reactions are performed with ethyl iodoacetate as a nucleophile and Me2Zn as the zinc source. The presence of air was found to be crucial to achieve an effective C-C bond formation pointing to a radical mechanism.

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University of Groningen Digital Archive

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Last time updated on 06/08/2013

This paper was published in University of Groningen Digital Archive.

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