Use of biological systems for the synthesis of chiral molecules. 5. Microbiological reduction of acyclic .beta.-diketones
- 1 October 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (22) , 5215-5219
- https://doi.org/10.1021/jo00257a004
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Use of biological systems for the preparation of chiral molecules. 3. Application in pheromone synthesis: preparation of sulcatol enantiomersThe Journal of Organic Chemistry, 1987
- Regio- and Enantio-selective Reduction ofα,γ-Diketones by Fermenting Bakers’ YeastAgricultural and Biological Chemistry, 1986
- Enantiospecific synthesis of optically pure (S)-(+)-3-hydroxy-1-phenyl-1-butanone by bakers' yeast reductionCanadian Journal of Chemistry, 1986
- Thermostable enzymes in organic synthesis. 2. Asymmetric reduction of ketones with alcohol dehydrogenase from Thermoanaerobium brockiiJournal of the American Chemical Society, 1986
- Synthese von endo‐ und exo‐1,3‐Dimethyl‐2,9‐dioxa‐bicyclo[3.3.1]nonanHelvetica Chimica Acta, 1977