Microbial reduction of varying size cyclic β-ketoesters. Stereoselective synthesis of chiral lactones and epoxides

Journal of Molecular Catalysis - B Enzymatic

Volumn 5, Issue 1-4, 1998, Pages 255-259

  Danchet, Sylvie ^a   Buisson, Didier ^a   Azerad, Robert ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Hydroxyester; Epoxyester; 1 Cyclobutanol 2 carboxylate; Diastereoselectivity; Dynamic kinetic resolution; Enantiospecificity

Indexed keywords

1 CYCLOBUTANOL 2 CARBOXYLATE; BETA HYDROXYESTER; CYCLOBUTANONE DERIVATIVE; EPOXIDE; ESTER DERIVATIVE; LACTONE; OMEGA EPOXYESTER; UNCLASSIFIED DRUG;

CHIRALITY; CONFERENCE PAPER; ENANTIOMER; NONHUMAN; REDUCTION; RHIZOPUS; SACCHAROMYCES CEREVISIAE; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032530464     PISSN: 13811177     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1381-1177(98)00045-9     Document Type: Conference Paper

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