Microbial reduction of 2-chloro-3-aryl-3-oxopropionic acid esters
- 24 November 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (48) , 7337-7340
- https://doi.org/10.1016/s0040-4039(00)60181-8
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Enantioselective synthesis of calcium channel blockers of the diltiazem groupThe Journal of Organic Chemistry, 1992
- Highly enantioselective routes to darzens and acetate aldol products from achiral aldehydes and t-butyl bromoacetateTetrahedron Letters, 1991
- Baker's yeast mediated transformations in organic chemistryChemical Reviews, 1991
- An improved synthesis of the taxol side chain and of RP 56976The Journal of Organic Chemistry, 1990
- Chemo-enzymatic synthesis of all isomeric 3-phenylserines and -isoserinesTetrahedron, 1990
- Baker's Yeast as a Reagent in Organic SynthesisSynthesis, 1990
- A Convenient Synthesis of Enantiomerically Pure (2R,3S)- and (2S,3R)-3-Hydroxy-2-methylbutanoic EstersSynthesis, 1988
- A Model For Predicting Diastereoselectivity In Yeast ReductionsBiocatalysis, 1987
- Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]Angewandte Chemie International Edition in English, 1984
- Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivativesAustralian Journal of Chemistry, 1976