Enantioselective Synthesis of Cyclopropanes by Aldehyde Homologation
Christina A. Risatti, Richard E. Taylor
Abstract
Christina A. Risatti, Richard E. Taylor
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).
Key concepts: Enantioselective synthesis, Aldehyde, Chemistry, Combinatorial chemistry, Stereochemistry, Organic chemistry, Catalysis