Bioconversion of organosilicon compounds by horse liver alcohol dehydrogenase: the role of the silicon atom in enzymatic reactions
- 1 October 1991
- journal article
- Published by Springer Nature in Applied Microbiology and Biotechnology
- Vol. 36 (1) , 40-43
- https://doi.org/10.1007/bf00164696
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Efficient optical resolution of 2-(4-chlorophenoxy)propanoic acid with lipase by the use of organosilicon compounds as substrate: the role of silicon atom in enzymatic recognitionJournal of Biotechnology, 1991
- Enantioselective reduction of acetyldimethylphenylsilane: A screening with thirty strains of microorganismsBiotechnology Letters, 1988
- Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindionesJournal of the American Chemical Society, 1988
- Enantioselective reduction of acetyldimethylphenylsilane by Trigonopsis variabilis (DSM 70714)Applied Microbiology and Biotechnology, 1987
- Enzymes as Catalysts in Synthetic Organic Chemistry [New Synthetic Methods (53)]Angewandte Chemie International Edition in English, 1985
- Structure of a triclinic ternary complex of horse liver alcohol dehydrogenase at 2.9 Å resolutionJournal of Molecular Biology, 1981
- Tilden Lecture. Some uses of silicon compounds in organic synthesisChemical Society Reviews, 1981
- Trends in Organosilicon Biological ResearchPublished by Elsevier ,1980
- Structure of Liver Alcohol Dehydrogenase at 2.9-Å ResolutionProceedings of the National Academy of Sciences, 1973