Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids
Author:
Affiliation:
1. Unilever Centre For Molecular Science Informatics, Department of Chemistry, Lensfield Road, Cambridge CB2 1EW, U.K.
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja800793t
Reference60 articles.
1. Brønsted Acid Catalysis: Organocatalytic Hydrogenation of Imines
2. Metal-Free Brønsted Acid Catalyzed Transfer Hydrogenation - New Organocatalytic Reduction of Quinolines
3. A selective reductive amination of aldehydes by the use of Hantzsch dihydropyridines as reductant
4. Asymmetric organocatalytic reductions mediated by dihydropyridines
5. Recent Developments in Asymmetric Transfer Hydrogenation with Hantzsch Esters: A Biomimetic Approach
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