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

Applied Microbiology and Biotechnology

Volumn 97, Issue 24, 2013, Pages 10329-10337

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

^a CHANGZHOU UNIVERSITY   (China)

^b EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

(S) phenyl methyl sulfoxide; Asymmetric oxidation; Biphasic system; CCZU10 1; Phenyl methyl sulfide; Rhodococcus sp

Indexed keywords

(S)-PHENYL METHYL SULFOXIDE; ASYMMETRIC OXIDATION; BIPHASIC SYSTEMS; CCZU10-1; PHENYL METHYL SULFIDE; RHODOCOCCUS SP;

ENANTIOSELECTIVITY; OXIDATION;

SULFUR COMPOUNDS;

OCTANE; SULFIDE; SULFONE; SULFOXIDE; THIOANISOLE; UNCLASSIFIED DRUG; WATER;

BACTERIUM; ENZYME ACTIVITY; OXIDATION;

AQUEOUS SOLUTION; ARTICLE; BIOCATALYST; CHEMICAL REACTION; ENANTIOSELECTIVITY; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATION; RHODOCOCCUS; WATER SUPPLY;

BIOTRANSFORMATION; OCTANES; OXIDATION-REDUCTION; RHODOCOCCUS; SOLVENTS; STEREOISOMERISM; SULFIDES; SULFOXIDES; WATER;

EID: 84892156399     PISSN: 01757598     EISSN: 14320614     Source Type: Journal    
DOI: 10.1007/s00253-013-5258-2     Document Type: Article

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