Highly enantioselective oxidation of phenyl methyl sulfide and its derivatives into optically pure (S)-sulfoxides with Rhodococcus sp. CCZU10-1 in an n-octane–water biphasic system-Reference-Cited by-同舟云学术

Highly enantioselective oxidation of phenyl methyl sulfide and its derivatives into optically pure (S)-sulfoxides with Rhodococcus sp. CCZU10-1 in an n-octane–water biphasic system

Published:2013-10-05 Issue:24 Volume:97 Page:10329-10337
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

He Yu-Cai,Ma Cui-Luan,Yang Zhen-Xing,Zhou Min,Xing Zhen,Ma Jiang-Tao,Yu Hui-Lei

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s00253-013-5258-2.pdf

Reference36 articles.

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2. Adam W, Korb MN, Roschmann KJ, Saha-Möller CR (1998) Titanium-catalyzed, asymmetric sulfoxidation of alkyl aryl sulfides with optically active hydroperoxides. J Org Chem 63:3423–3428

3. Beecher J, Richardson P, Roberts S, Willetts A (1992) Oxidative biotransformations by microorganisms: stereoselective sulfoxide formation by Saccharomyces cerevisiae. Biotechnol Lett 17:1069–1074

4. Beecher J, Richardson P, Willetts A (1994) Baeyer-Villiger monooxygenase-dependent biotransformations: stereospecific heteroatom oxidations by camphorgrown Pseudomonas putida to produce chiral sulfoxides. Biotechnol Lett 16:909–912

5. Bolm C, Simic O (2001) Highly enantioselective Hetero–Diels–Alder reactions catalyzed by a C2-symmetric bis (sulfoximine) copper (II) complex. J Am Chem Soc 123:3830–3831

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