Horse Liver Alcohol Dehydrogenase: An Illustrative Example of the Potential of Enzymes in Organic Synthesis
- 1 January 1982
- book chapter
- Published by Springer Nature
Abstract
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This publication has 15 references indexed in Scilit:
- Stereochemical nonequivalence of ligands and faces (heterotopicity)Journal of Chemical Education, 1980
- Preparation of useful chiral lactone synthons via stereospecific enzyme-catalysed oxidations of meso-diolsJournal of the Chemical Society, Chemical Communications, 1980
- Enzymes in organic synthesis. 16. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Stereospecific reductions of 2-substituted tetrahydrothiopyran-4-onesJournal of the American Chemical Society, 1979
- Large-scale enzyme-catalyzed synthesis of ATP from adenosine and acetyl phosphate. Regeneration of ATP from AMPJournal of the American Chemical Society, 1978
- Hydroxymethylbenzimidazole carboxylic acid models of the Asp-His-Ser charge relay system of serine proteasesCanadian Journal of Chemistry, 1977
- Regiospecific and enantioselective horse liver alcohol dehydrogenase catalyzed oxidations of some hydroxycyclopentanesJournal of the American Chemical Society, 1977
- Enzyme discrimination between conformational enantiomers as a means of effecting asymmetric synthesesJournal of the Chemical Society, Chemical Communications, 1977
- Studies of enzyme-mediated reactions. Part VII. Stereospecific syntheses of tritium-labelled (2R)- and (2S)-dopamines: stereochemical course of hydroxylation of dopamine by dopamine β-hydroxylase (E.C. 1.14.17.1)Journal of the Chemical Society, Perkin Transactions 1, 1976
- Structure of the primary acid rearrangement product of reduced nicotinamide adenine dinucleotide (NADH)Biochemistry, 1974