Substrate modification as a means of enhancing the enantioselectivity of microbial reductions of .beta.-keto esters. A (R)- or (S)-1,3,5-trihydroxypentane synthon
- 1 January 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (2) , 192-196
- https://doi.org/10.1021/jo00378a007
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Enzymes in organic synthesis. 35. Stereoselective pig liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters. Optimization of enantiomeric excess via reaction conditions controlThe Journal of Organic Chemistry, 1986
- Preparation by yeast reduction and determination of the sense of chirality of enantiomerically pure ethyl (−)-4,4,4-trichloro-3-hydroxy- and (+)-4,4,4-trifluoro-3-hydroxybutanoateHelvetica Chimica Acta, 1984
- Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]Angewandte Chemie International Edition in English, 1984
- Asymmetric Reductions. XII. Stereoselective Ketone Reductions by Fermenting Yeast*Biochemistry, 1964