Direct Asymmetric Reductive Amination
Author:
Affiliation:
1. Department of Process Research, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065, and Corporate Research & Development Division, Takasago International Corporation, 1-4-11 Nishi-yawata, Hiratsuka City, Kanagawa 254-0073, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja905143m
Reference19 articles.
1. Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids
2. Enantioselective Synthesis of β-Amino Acids
3. Metal−Brønsted Acid Cooperative Catalysis for Asymmetric Reductive Amination
4. The First Highly Enantioselective Homogeneously Catalyzed Asymmetric Reductive Amination: Synthesis of α-N-Benzylamino Acids
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