Highly enantioselective oxidation of racemic phenyl-1,2-ethanediol to optically pure (R)-(−)-mandelic acid by a newly isolated Brevibacterium lutescens CCZU12-1-Reference-Cited by-同舟云学术

Highly enantioselective oxidation of racemic phenyl-1,2-ethanediol to optically pure (R)-(−)-mandelic acid by a newly isolated Brevibacterium lutescens CCZU12-1

Published:2013-06-05 Issue:16 Volume:97 Page:7185-7194
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

He Yu-Cai,Ma Cui-Luan,Zhang Xian,Li Liang,Xu Jian-He,Wu Miao-Xin

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s00253-013-4989-4.pdf

Reference36 articles.

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4. Choi DS, Han SS, Kwueon EK (2006) New mono-quarternized bis-cinchona alkaloid ligands for asymmetric dihydroxylation of olefins in aqueous medium: unprecedented high enantioselectivity and recyclability. Adv Synth Catal 348:2560–2564

5. Chang L, Ouyang L, Xu Y, Pan J, Xu JH (2010) Highly enantioselective hydrolysis of phenyl-1,2-ethanediol cyclic carbonates. J Mol Catal B Enzym 66:95–100

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