Chiral cyclohexanoid synthetic precursors via asymmetricmicrobial reduction of prochiral cyclohexanediones
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (12) , 1241-1244
- https://doi.org/10.1016/s0040-4039(01)80123-4
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitineJournal of the American Chemical Society, 1983
- Total synthesis of the trichothecene mycotoxin anguidineJournal of the American Chemical Society, 1983
- Enantiospecific syntheses of trifunctional (R)-3-hydroxy esters by baker's yeast reductionJournal of the Chemical Society, Chemical Communications, 1983
- Chiral cyclopentanoid synthetic intermediates via asymmetric microbial reduction of prochiral 2,2-disubstituted cyclopentanedionesThe Journal of Organic Chemistry, 1982
- Mikrobielle Reduktion 2,2‐disubstituierter Cyclopentan‐1,3‐dione. Darstellung chiraler Cyclopentanderivate für die Synthese von 8‐Methyl‐prostaglandinenJournal für Praktische Chemie, 1981
- Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivativesAustralian Journal of Chemistry, 1976
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969
- Asymmetric Reductions. XII. Stereoselective Ketone Reductions by Fermenting Yeast*Biochemistry, 1964
- Untersuchungen an Diazomethanen, XIX1). Ring‐A‐Homologe SteroidhormoneEuropean Journal of Organic Chemistry, 1963
- The Reaction of Ketones with DiazomethaneJournal of the American Chemical Society, 1960