Organic letters

Microbial deracemization of α-substituted carboxylic acids

D Kato, S Mitsuda, H Ohta

Index: Kato, Dai-ichiro; Mitsuda, Satoshi; Ohta, Hiromichi Organic letters, 2002 , vol. 4, # 3 p. 371 - 373

Full Text: HTML

Citation Number: 36

Abstract

In this Letter, we report a preparation of optically active α-substituted carboxylic acids via a novel enzymatic deracemization reaction using whole cells. This deracemization reaction inverts the chirality of one enantiomer of a racemate to the other antipode, resulting in an optically active compound starting from a racemic mixture. Thus this process is entirely different from the above-mentioned dynamic resolution, 2 because in this reaction the starting material and ...

Related Articles:

Chlorination of 2-phenoxypropanoic acid with NCP in aqueous acetic acid: Using a novel ortho-para relationship and the para/meta ratio of substituent effects for …

[Segurado, Manuel A. P.; Reis, Joao Carlos R.; De Oliveira, Jaime D. Gomes; Kabilan, Senthamaraikannan; Shanthi, Manohar Journal of Organic Chemistry, 2007 , vol. 72, # 14 p. 5327 - 5336]

More Articles...