Enantioselective Enolate Protonation with Chiral Anilines: Scope, Structural Requirements, and Mechanistic Implications
Author:
Affiliation:
1. Contribution from the Chemistry Department, University of Wisconsin, Madison, Wisconsin 53706, and the Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja994437m
Reference31 articles.
1. Deracemization via Highly Enantioselective Enolate Protonation Using a Chiral Aniline as the "Acid"
2. Catalytic Asymmetric Protonation of Amide Enolates: Optimization of Kinetic Acidity in the Catalytic Cycle
3. Enantioselective Enolate Protonation: Matching Chiral Aniline and Substrate Acidity
4. Substituted Isoquinolines by Noyori Transfer Hydrogenation: Enantioselective Synthesis of Chiral Diamines Containing an Aniline Subunit
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