Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5269299 | Tetrahedron Letters | 2014 | 6 Pages |
Abstract
A method for the enantioselective synthesis of γ-lactones through the reaction of enantioenriched sulfoxonium ylides, aldehydes, and ketenes was developed. Enantioenriched (98% ee) aminosulfoxonium ylide was subjected to reaction with a variety of aldehydes (both aromatic and aliphatic) and disubstituted ketenes, leading to the formation of α,β-substituted γ-lactones in moderate to very good diastereoselectivity (dr up to 95:5) and with enantiomeric excesses of up to 79% ee.
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Authors
Nicholas J. Peraino, Han-Jen Ho, Mukulesh Mondal, Nessan J. Kerrigan,