New method for synthesizing the intermediates to 5-HETE from yeast-mediated reduction products by employing Baeyer-Villiger oxidation with complete retention of enantiomeric excess

Bioscience, Biotechnology and Biochemistry

Volumn 67, Issue 9, 2003, Pages 1959-1969

  Yamauchi, Satoshi ^a   Kinoshita, Yoshihiro ^a   Kinoshita, Yoshiro ^a  

^a EHIME UNIVERSITY   (Japan)

Author keywords

5 HETE; Yeast reduction

Indexed keywords

ALDEHYDE; CYCLOPENTANE DERIVATIVE; CYCLOPENTANONE; ESTER; GLYCOL; HYDROXYICOSATETRAENOIC ACID; KETONE; LACTONE;

ARTICLE; BIOSYNTHESIS; BIOTRANSFORMATION; CHEMISTRY; HYDROXYLATION; METABOLISM; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS; YEAST;

ALDEHYDES; BIOTRANSFORMATION; CYCLOPENTANES; ESTERS; GLYCOLS; HYDROXYEICOSATETRAENOIC ACIDS; HYDROXYLATION; KETONES; LACTONES; OXIDATION-REDUCTION; STEREOISOMERISM; YEASTS;

EID: 2842515900     PISSN: 09168451     EISSN: None     Source Type: Journal    
DOI: 10.1271/bbb.67.1959     Document Type: Article

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