Highly efficient conversion of (±)-mandelic acid to its (R)-(−)-enantiomer by combination of enzyme-mediated oxidation and reduction
- 1 December 1992
- journal article
- Published by Springer Nature in Biotechnology Letters
- Vol. 14 (12) , 1137-1142
- https://doi.org/10.1007/bf01027017
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Enantioselective oxidation of mandelic acid using a phenylmalonate metabolizing pathway of a soil bacteriumAlcaligenes bronchisepticus KU 1201Biotechnology Letters, 1992
- Asymmetric Decarboxylation of Disubstituted Malonic Acid by Alcaligenes bronchisepticus KU 1201Biocatalysis, 1991
- Enzyme-mediated asymmetric decarboxylation of disubstituted malonic acidsJournal of the American Chemical Society, 1990
- Membrane-bound lactate dehydrogenases and mandelate dehydrogenases of Acinetobacter calcoaceticus. Purification and propertiesBiochemical Journal, 1985
- Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure .alpha.-hydroxy carboxylic acid synthonsJournal of the American Chemical Society, 1985
- Mutant strains of Acinetobacter calcoaceticus possessing additional mandelate dehydrogenases. Identification and preliminary characterization of the enzymesBiochemical Journal, 1983
- Enzymic conversion of .alpha.-keto aldehydes to optically active .alpha.-hydroxy acids using glyoxalase I and IIThe Journal of Organic Chemistry, 1981
- Synthesis of optically active alkynyl alcohols and α-hydroxy esters by microbial asymmetric hydrolysis of the corresponding acetatesTetrahedron, 1980
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976