Enzymes in organic synthesis. 37. Preparation and characterization of potential decalindione substrates of horse liver alcohol dehydrogenase
- 1 October 1987
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 65 (10) , 2397-2404
- https://doi.org/10.1139/v87-400
Abstract
The preparations of ten decalindiones for investigation as substrates of horse liver alcohol dehydrogenase are reported. The structure characterizations include clarifications of some ambiguities in the decalin literature.This publication has 4 references indexed in Scilit:
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- 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 diolsJournal of the American Chemical Society, 1984
- 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
- Stereoselective horse liver alcohol dehydrogenase catalyzed oxidoreductions of some bicyclic [2.2.1] and [3.2.1] ketones and alcoholsJournal of the American Chemical Society, 1976