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Formation of chiral quaternary carbon stereocenters using silylene transfer reactions: enantioselective synthesis of (+)-5-epi-acetomycin
Authors:Calad Stacie A  Woerpel K A
Affiliation:Department of Chemistry, University of California, Irvine, CA 92627-2025, USA.
Abstract:Chiral quaternary carbon stereocenters can be established with high diastereoselectivity by a silylene transfer/Ireland-Claisen rearrangement. The utility of this method was demonstrated by application to a synthesis of (+)-5-epi-acetomycin. [reaction: see text]
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