Asymmetric microbial reduction of prochiral 2,2,-disubstituted cycloalkanediones
- 1 July 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (15) , 3223-3232
- https://doi.org/10.1021/jo00391a009
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Substrate modification as a means of enhancing the enantioselectivity of microbial reductions of .beta.-keto esters. A (R)- or (S)-1,3,5-trihydroxypentane synthonThe Journal of Organic Chemistry, 1987
- Synthetic approach to versatile chiral molecules containing a fluorine atomThe 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
- BIOCHEMISTRY OF THE USTILAGINALES: IV. THE CONFIGURATIONS OF SOME β–HYDROXYACIDS AND THE BIOREDUCTION OF β–KETOACIDSCanadian Journal of Chemistry, 1951