Practical Syntheses of Chiral α-Amino Acids and Chiral Half-Esters by Kinetic Resolution of Urethane-Protected α-Amino Acid N-Carboxyanhydrides and Desymmetrization of Cyclic meso-Anhydrides with New Modified Cinchona Alkaloid Catalysts-Reference-Cited by-同舟云学术

Practical Syntheses of Chiral α-Amino Acids and Chiral Half-Esters by Kinetic Resolution of Urethane-Protected α-Amino Acid N-Carboxyanhydrides and Desymmetrization of Cyclic meso-Anhydrides with New Modified Cinchona Alkaloid Catalysts

Published:2007-04-19 Issue:3 Volume:11 Page:609-615
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Ishii Yutaka¹,Fujimoto Ryosuke¹,Mikami Masafumi¹,Murakami Satoshi¹,Miki Yasushi¹,Furukawa Yoshiro¹

Affiliation:

1. Research Laboratories, Daiso Co., Ltd., 9-Otakasu-cho, Amagasaki-shi 660-0842, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op700023h

Reference28 articles.

1. In the Golden Age of Organocatalysis

2. Asymmetric Organocatalysis

3. Control of Diastereoselectivity in Tandem Asymmetric Reactions Generating Nonadjacent Stereocenters with Bifunctional Catalysis by Cinchona Alkaloids

4. A Highly Enantioselective Catalytic Desymmetrization of Cyclic Anhydrides with Modified Cinchona Alkaloids

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