Stereochemistry of horse liver alcohol dehydrogenase mediated oxidoreduction of 2-brendanone type cage-shaped tricyclic ketones and the related stereoisomeric alcohols
- 1 November 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 48 (23) , 4337-4345
- https://doi.org/10.1021/jo00171a036
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Stereochemistry of horse liver alcohol dehydrogenase (HLADH) mediated oxidoreduction in cage-shaped carbonyl compoundsThe Journal of Organic Chemistry, 1983
- C2-ketone rule in horse liver alcohol dehydrogenase (HLADH) mediated oxidoreductionThe Journal of Organic Chemistry, 1981
- Synthesis and absolute configuration of optically active D3-tritwistane; the gyrochiral prototype of "twist" diamondThe Journal of Organic Chemistry, 1981
- Microbial stereodifferentiating reduction of 2,6-adamantanedione and hexahydrodibenzoheptalene-5,11-dione, diketones with two homotopic carbonyl groups on a C2 symmetry axisThe Journal of Organic Chemistry, 1981
- Microbial stereodifferentiating reduction of carbonyl compounds; proposed quadrant ruleThe 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
- Syntheses and chiroptical properties of (+)-2-brendanone and its analogsThe Journal of Organic Chemistry, 1979