Kinetic Resolution of Racemic α-Arylalkanoic Acids with Achiral Alcohols via the Asymmetric Esterification Using Carboxylic Anhydrides and Acyl-Transfer Catalysts-Reference-Cited by-同舟云学术

Kinetic Resolution of Racemic α-Arylalkanoic Acids with Achiral Alcohols via the Asymmetric Esterification Using Carboxylic Anhydrides and Acyl-Transfer Catalysts

Published:2010-08-03 Issue:33 Volume:132 Page:11629-11641
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Shiina Isamu¹,Nakata Kenya¹,Ono Keisuke¹,Onda Yu-suke¹,Itagaki Makoto¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1−3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan, and Organic Synthesis Research Laboratory, Sumitomo Chemical Co., Ltd., 1−98 Kasugade-naka, 3-chome, Konohana-ku, Osaka 554-8558, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja103490h

Reference51 articles.

1. For reviews of routes to optically active arylpropanoic acids, see:

2. Recent developments in the synthesis of optically active α-arylpropanoic acids: An important class of non-steroidal anti-inflammatory agents

3. Tetrahedron report number 205

4. Enantioselective Addition of Alcohols to Ketenes Catalyzed by a Planar-Chiral Azaferrocene: Catalytic Asymmetric Synthesis of Arylpropionic Acids

5. Enantioselective Addition of Amines to Ketenes Catalyzed by a Planar-Chiral Derivative of PPY: Possible Intervention of Chiral Brønsted-Acid Catalysis

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