Highly Stereoselective Oxy-Michael Additions to β,γ-Unsaturated α-Keto Esters: Rapid Enantioselective Synthesis of 3-Hydroxybutenolides
Author:
Affiliation:
1. School of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol702693m
Reference23 articles.
1. (b) Buchanan, D. J.; Dixon, D. J.; Scott, M. S.; Lainé, D. I.Tetrahedron: Asymmetry2004,15, 195−197.
2. Highly Stereoselective Intermolecular Oxy-Michael Addition Reaction to α,β-Unsaturated Malonate Esters
3. Highly stereoselective oxy-Michael additions to α,β-disubstituted nitro olefins: asymmetric synthesis of pseudo-norephedrine derivatives and THP* protected α-hydroxy ketones
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