Absolute Configuration of Optically Active Tricyclo[2.2.1.02,6]heptan-3-ol (Nortricyclanol). An Enhancement of Enantiomeric Purity of a Chiral Alcohol by Repeating Enzymatic Kinetic Resolution
- 1 November 1989
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 18 (11) , 1939-1942
- https://doi.org/10.1246/cl.1989.1939
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The Cyclopropyl Group in Studies of Enzyme Mechanism and InhibitionAngewandte Chemie International Edition in English, 1988
- Tetrahedron report number 203Tetrahedron, 1986
- Enzymes as Catalysts in Synthetic Organic Chemistry [New Synthetic Methods (53)]Angewandte Chemie International Edition in English, 1985
- Stereochemistry of horse liver alcohol dehydrogenase (HLADH) mediated oxidoreduction in cage-shaped carbonyl compoundsThe Journal of Organic Chemistry, 1983
- Mechanistic probes of the hydride-transfer process in the NADH-dependent alcohol dehydrogenase reactionsThe Journal of Organic Chemistry, 1982
- C2-ketone rule in horse liver alcohol dehydrogenase (HLADH) mediated oxidoreductionThe Journal of Organic Chemistry, 1981
- [10] Fatty acid synthase from pig liverPublished by Elsevier ,1981
- Microbial stereodifferentiating reduction of the carbonyl groups located on the C2 axes of gyrochiral moleculesThe Journal of Organic Chemistry, 1979
- 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
- Memory effects in multiple carbonium ion rearrangements. IV. Solvolytic studies of the tricyclo[3.2.1.02,7]oct-4-yl systemJournal of the American Chemical Society, 1969