Stereochemical control of microbial reduction. 2. Reduction of β-keto esters by immobilized bakers' yeast
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (35) , 4213-4216
- https://doi.org/10.1016/s0040-4039(00)98995-0
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Preparative Microbial Reduction of β‐Oxoesters with Thermoanaerobium brockiiAngewandte Chemie International Edition in English, 1984
- Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitineJournal of the American Chemical Society, 1983
- Enantiospecific syntheses of trifunctional (R)-3-hydroxy esters by baker's yeast reductionJournal of the Chemical Society, Chemical Communications, 1983
- A chiral total synthesis of compactinJournal of the American Chemical Society, 1982
- Stereospezifische Synthese von (+)‐(3R, 4R)‐4‐Methyl‐3‐heptanol, das Enantiomere eines Pheromons des kleinen Ulmensplintkäfers (Scolytus multistriatus)Helvetica Chimica Acta, 1979
- Hydrophilic urethane prepolymers: Convenient materials for enzyme entrapmentBiotechnology & Bioengineering, 1978
- The immobilization of microbial cells, subcellular organelles, and enzymes in calcium alginate gelsBiotechnology & Bioengineering, 1977
- Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivativesAustralian Journal of Chemistry, 1976
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969
- BIOCHEMISTRY OF THE USTILAGINALES: IV. THE CONFIGURATIONS OF SOME β–HYDROXYACIDS AND THE BIOREDUCTION OF β–KETOACIDSCanadian Journal of Chemistry, 1951