The First Stereoselective Ficini−Claisen Rearrangement Using Chiral Ynamides
Author:
Affiliation:
1. Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol020037j
Reference47 articles.
1. Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. A Highly Stereoselective Synthesis of Acrylic Acid Derivatives and 1,3-Dienes Using an Electron Deficient Variant of Ynamine
2. The First Epoxidations of 1-Amidoallenes. A General Entry to Nitrogen-Substituted Oxyallyl Cations in Highly Stereoselective [4 + 3] Cycloadditions
3. Reaction of Secondary Acetamides withN-Dichloromethylene-N,N-dimethylammonium Chloride
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