A Highly Enantioselective Route to Either Enantiomer of Both α- and β-Amino Acid Derivatives-Reference-Cited by-同舟云学术

A Highly Enantioselective Route to Either Enantiomer of Both α- and β-Amino Acid Derivatives

Published:2002-02-08 Issue:9 Volume:124 Page:1866-1867
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Córdova Armando¹,Watanabe Shin-ichi¹,Tanaka Fujie¹,Notz Wolfgang¹,Barbas Carlos F.¹

Affiliation:

1. The Skaggs Institute for Chemical Biology and the Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja017833p

Reference33 articles.

1. α-Oxymethyl Ketone Enolates for the Asymmetric Mannich Reaction. From Acetylene andN-Alkoxycarbonylimines toβ-Amino Acids

2. Mechanism of Palladium Complex-Catalyzed Enantioselective Mannich-Type Reaction: Characterization of A Novel Binuclear Palladium Enolate Complex

3. Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst for the Synthesis of Optically Active β-Amino Acid Derivatives

4. A New Chiral BLA Promoter for Asymmetric Aza Diels-Alder and Aldol-Type Reactions of Imines

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