Amanote Research
Register
Sign In
The Mannich Reaction of Malonates With Simple Imines Catalyzed by Bifunctional Cinchona Alkaloids: Enantioselective Synthesis of Β-Amino Acids
Journal of the American Chemical Society
- United States
doi 10.1021/ja060716f
Full Text
Open PDF
Abstract
Available in
full text
Categories
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Date
May 1, 2006
Authors
Jun Song
Yi Wang
Li Deng
Publisher
American Chemical Society (ACS)
Related search
The Mannich Reaction of Malonates With Simple Imines Catalyzed by Bifunctional Cinchona Alkaloids: Enantioselective Synthesis of B-Amino Acids
The Mannich Reaction of Malonates With Simple Imines Catalyzed by Bifunctional Cinchona Alkaloids: Enantioselective Synthesis of B-Amino Acids
Bifunctional Iminophosphorane Catalyzed Enantioselective Ketimine Phospha-Mannich Reaction
Synlett
Organic Chemistry
Organocatalytic Enantioselective Mannich Reaction: Direct Access to Chiral Β-Amino Esters
ACS Omega
Chemistry
Chemical Engineering
Bifunctional ThioureaAmmonium Salt Catalysts Derived From Cinchona Alkaloids: Cooperative Phase-Transfer Catalysts in the Enantioselective Aza-Henry Reaction of Ketimines
Selective Synthesis of Β-Amino Esters and Β-Lactams by Rhodium-Catalyzed Reformatsky-Type Reaction
Heterocycles
Organic Chemistry
Analytical Chemistry
Pharmacology
Catalytic Enantioselective Synthesis of Chiral 3-Amino-2-Oxindoles by a Mannich Approach
Synlett
Organic Chemistry
Efficient Synthesis of B2-Amino Acid by Homologation of A-Amino Acids Involving the Reformatsky Reaction and Mannich-Type Imminium Electrophile
Rhodium-Catalyzed Enantioselective Hydrogenation of B-Phthalimide Acrylates to Synthesis of B2-Amino Acids
