Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindiones
- 1 January 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 110 (2) , 577-583
- https://doi.org/10.1021/ja00210a044
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Enzymes in organic synthesis. 16. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Stereospecific reductions of 2-substituted tetrahydrothiopyran-4-onesJournal of the American Chemical Society, 1979
- The Stereochemistry of the Conversion of D and L 1,2-Propanediols to PropionaldehydeJournal of Biological Chemistry, 1966