Enzymes in organic synthesis. 31. Preparations of enantiomerically pure bicyclic [3.2.1] and [3.3.1] chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of meso diols
- 1 March 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 106 (5) , 1461-1467
- https://doi.org/10.1021/ja00317a046
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Stereochemical Aspects of the Substrate Specificity of Horse Liver Alcohol Dehydrogenase*Biochemistry, 1965
- Specification of the stereospecificity of some oxido-reductases by diamond lattice sectionsPure and Applied Chemistry, 1964