Selective inhibition of R-enzymes by simple organic acids in yeast-catalysed reduction of ethyl 3-oxobutanoate
- 31 October 1991
- journal article
- Published by Elsevier in Enzyme and Microbial Technology
- Vol. 13 (10) , 834-839
- https://doi.org/10.1016/0141-0229(91)90068-l
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Synthesis of optically active pheromonesTetrahedron, 1989
- Highly diastereoselective diels-alder reaction of optically active 2-p-tolylsulphinyl-2-cycloalkenones with cyclopentadieneTetrahedron Letters, 1989
- An asymmetric synthesis of carbapenem antibiotic (+)-PS-5 from ethyl 3-hydroxybutanoateThe Journal of Organic Chemistry, 1988
- Complete stereoselective synthesis of chiral intermediates for thienamycin and related antibioticsJournal of the Chemical Society, Chemical Communications, 1988
- A FACILE, STEREOCONTROLLED ENTRY TO KEY INTERMEDIATES FOR THIENAMYCIN SYNTHESIS FROM ETHYL (S)-3-HYDROXYBUTANOATEChemistry Letters, 1985
- A novel synthetic method for α-methylene-γ-butyrolactonesTetrahedron Letters, 1984
- Ethyl (S)-3-Hydroxybutanoate as a Starting Material for the Synthesis of (S)-(-)-Citronellol and other Chiral AlcoholsSynthesis, 1982
- Stereochemistry of Friedel-Crafts Reaction of Benzene with Optically Active 2-MethyloxetaneBulletin of the Chemical Society of Japan, 1982
- A simple synthesis of (S)-(+)-sulcatol, the pheromone of gnathotrichus retusus, employing baker's yeast for asymmetric reductionTetrahedron, 1981
- Studies directed toward the total synthesis of streptogramin antibiotics. Enantiospecific approach to the nine-membered macrocycle of griseoviridinJournal of the American Chemical Society, 1980