Enzymes in organic synthesis. 46. Regiospecific and stereoselective horse liver alcohol dehydrogenase catalyzed reductions of cis- and trans-bicyclo[4.3.0]nonanones
- 1 April 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (8) , 1795-1801
- https://doi.org/10.1021/jo00269a010
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindionesJournal of the American Chemical Society, 1988
- Determination of the absolute configuration of six-membered-ring ketones by carbon-13 NMRJournal of the American Chemical Society, 1987
- 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 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
- Crystallography of liver alcohol dehydrogenase complexed with substratesJournal of Molecular Biology, 1978
- Regiospecific and enantioselective horse liver alcohol dehydrogenase catalyzed oxidations of some hydroxycyclopentanesJournal of the American Chemical Society, 1977
- The Stereochemistry of the Conversion of D and L 1,2-Propanediols to PropionaldehydeJournal of Biological Chemistry, 1966