Enzymes in organic synthesis. 25. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Highly stereoselective reductions of 2-substituted tetrahydropyran-4-ones
- 1 August 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 104 (17) , 4666-4671
- https://doi.org/10.1021/ja00381a025
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of monocyclic meso diolsJournal of the American Chemical Society, 1982
- Enzymes in organic syntheses. 19. Evaluation of the stereoselectivities of horse liver alcohol dehydrogenase; catalyzed oxidoreductions of hydroxy- and ketothiolanes, -thianes, and -thiepanesCanadian Journal of Chemistry, 1981
- C2-ketone rule in horse liver alcohol dehydrogenase (HLADH) mediated oxidoreductionThe Journal of Organic Chemistry, 1981
- 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
- Enzymes in organic synthesis. 14. Stereoselective horse liver alcohol dehydrogenase catalyzed oxidations of diols containing a prochiral centre and of related hemiacetalsCanadian Journal of Chemistry, 1979
- 3-Substituted pyrazole derivatives as inhibitors and inactivators of liver alcohol dehydrogenaseJournal of Medicinal Chemistry, 1979
- The Stereochemistry of the Conversion of D and L 1,2-Propanediols to PropionaldehydeJournal of Biological Chemistry, 1966