4-Aryloxybutenolides As “Chiral Aldehyde” Equivalents: An Efficient Enantioselective Synthesis of (+)-Brefeldin A
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja026438b
Reference18 articles.
1. α-Acetoxysulfones as “Chiral Aldehyde” Equivalents
2. Palladium-Catalyzed Kinetic and Dynamic Kinetic Asymmetric Transformation of 5-Acyloxy-2-(5H)-furanone. Enantioselective Synthesis of (−)-Aflatoxin B Lactone
3. Straightforward Synthesis of Isopropylidenediphenylsulfurane and Application to Industrially Viable Stereoselective Synthesis of Deltamethrin Insecticide
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