2004Angewandte Chemie International EditionRequires access

Enantioselective Synthesis of Cyclopropanes by Aldehyde Homologation

Christina A. Risatti, Richard E. Taylor

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Abstract

An efficient method for the enantioselective preparation of structurally diverse cyclopropanes has been developed. Sequential homoaldol coupling and activation steps result in a three-carbon homologation of an aldehyde to give a nonracemic, stereochemically rich cyclopropylcarboxaldehyde (see scheme).

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An efficient method for the enantioselective preparation of structurally diverse cyclopropanes has been developed. Sequential homoaldol coupling and activation steps result in a three-carbon homologation of an aldehyde to give a nonracemic, stereochemically rich cyclopropylcarboxaldehyde (see scheme).

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Available abstract

An efficient method for the enantioselective preparation of structurally diverse cyclopropanes has been developed. Sequential homoaldol coupling and activation steps result in a three-carbon homologation of an aldehyde to give a nonracemic, stereochemically rich cyclopropylcarboxaldehyde (see scheme).

Key concepts: Enantioselective synthesis, Aldehyde, Chemistry, Combinatorial chemistry, Stereochemistry, Organic chemistry, Catalysis

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