C2-ketone rule in horse liver alcohol dehydrogenase (HLADH) mediated oxidoreduction
- 1 June 1981
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 46 (13), 2726-2730
- https://doi.org/10.1021/jo00326a025
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Microbial stereodifferentiating reduction of carbonyl compounds; proposed quadrant ruleThe Journal of Organic Chemistry, 1980
- Microbial stereodifferentiating reduction of (.+-.)-4-methyl- and (.+-.)-6-methyl-1-oxo[2.2]metacyclophanes and revision of the absolute configuration of 4-substituted [2.2]metacyclophanesThe Journal of Organic Chemistry, 1980
- Microbial stereodifferentiating reduction of the carbonyl groups located on the C2 axes of gyrochiral moleculesThe Journal of Organic Chemistry, 1979
- 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
- Microbial stereodifferentiating reduction in [2.2]metacyclophane derivativesThe Journal of Organic Chemistry, 1979
- Regiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanesCanadian Journal of Chemistry, 1977
- Regiospecific and enantioselective horse liver alcohol dehydrogenase catalyzed oxidations of some hydroxycyclopentanesJournal of the American Chemical Society, 1977
- Asymmetric syntheses via enantiotopically selective horse liver alcohol dehydrogenase catalyzed oxidations of diols containing a prochiral centerJournal of the American Chemical Society, 1977
- 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
- Specification of the stereospecificity of some oxido-reductases by diamond lattice sectionsPure and Applied Chemistry, 1964