Determination of the absolute configuration of six-membered-ring ketones by carbon-13 NMR
- 1 March 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 109 (5), 1363-1370
- https://doi.org/10.1021/ja00239a013
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Enzymes in organic synthesis. 27. Horse liver alcohol dehydrogenase-catalyzed oxidoreductions of 3-alkylthiopyran ketones and alcoholsThe Journal of Organic Chemistry, 1983
- Enzymes in organic synthesis. 28. Reinvestigation of the horse liver alcohol dehydrogenase-catalyzed reductions of 2-alkylcyclohexanones.Identification of cis-alkylcyclohexanols as minor productsCanadian Journal of Chemistry, 1982
- Enzymes in organic synthesis. 25. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Highly stereoselective reductions of 2-substituted tetrahydropyran-4-onesJournal 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