Chiral Lewis Acid-Catalyzed Highly Enantioselective [4 + 3] Cycloaddition Reactions of Nitrogen-Stabilized Oxyallyl Cations Derived from Allenamides
Author:
Affiliation:
1. Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja044760b
Reference28 articles.
1. The Emergence of Allenamides in Organic Synthesis
2. Synthesis of 1-Deoxy-d-galactohomonojirimycin via Enantiomerically Pure Allenylstannanes
3. Inverse electron-demand aza-[4+2] cycloaddition reactions of allenamides
4. The First Epoxidations of 1-Amidoallenes. A General Entry to Nitrogen-Substituted Oxyallyl Cations in Highly Stereoselective [4 + 3] Cycloadditions
5. A Tandem Epoxidation/Stereoselective Intramolecular[4+3] Cycloaddition Reaction Involving Nitrogen-Stabilized Oxyallyl Cations Derived from Chiral Allenamides
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