Enantioselective microbial reduction of 3,5-dioxo-6-(benzyloxy) hexanoic acid, ethyl ester
Authors:
- Ramesh N. PatelRPRamesh N. Patel
- Amit BanerjeeABAmit Banerjee
- Clyde G. McNameeCMClyde G. McNamee
- David BrzozowskiDBDavid Brzozowski
- Ronald L. HansonRHRonald L. Hanson
- Laszlo J. SzarkaLSLaszlo J. Szarka
- 1 December 1993
- journal article
- Published by Elsevier in Enzyme and Microbial Technology
- Vol. 15 (12) , 1014-1021
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Stereoselective reduction of β-keto esters by Geotrichum candidumEnzyme and Microbial Technology, 1992
- Baker's yeast mediated transformations in organic chemistryChemical Reviews, 1991
- Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitorsJournal of Medicinal Chemistry, 1990
- Reductive biotransformations of organic compounds by cells or enzymes of yeastEnzyme and Microbial Technology, 1990
- Dehydrogenases for the synthesis of chiral compoundsEuropean Journal of Biochemistry, 1989
- Biochemical preparations of both the enantiomers of methyl 3-hydroxypentanoate and their conversion to the enantiomers of 4-hexanolide, the pheromone of trogoderma glabrumTetrahedron, 1985
- Preparation of chiral cyclohexanol derivative with high optical purity by yeast reductionTetrahedron Letters, 1985
- Mikrobielle asymmetrische Katalyse — enantioselektive Reduktion von KetonenAngewandte Chemie, 1984
- Bifunctional chiral synthons via biochemical methods. 5. Preparation of (S)-ethyl hydrogen-3-hydroxyglutarate, key intermediate to (R)-4-amino-3-hydroxybutyric acid and L-carnitine.Tetrahedron Letters, 1984
- A chiral total synthesis of compactinJournal of the American Chemical Society, 1982