ChemInform Abstract: Thermostable Enzymes in Organic Synthesis. Part 2. Asymmetric Reduction of Ketones with Alcohol Dehydrogenase from Thermoanaerobium brockii

1986 ◽  
Vol 17 (19) ◽  
Author(s):  
E. KEINAN ◽  
E. K. HAFELI ◽  
K. K. SETH ◽  
R. LAMED
1984 ◽  
Vol 62 (11) ◽  
pp. 2578-2582 ◽  
Author(s):  
J. Bryan Jones ◽  
Christopher J. Francis

Preparative-scale horse liver alcohol dehydrogenase-catalyzed oxidation of mesoexo- and endo-7-oxabicyclo[2.2.1]heptane diols provides a direct one-step route to enantiomerically pure chiral γ-lactones of the oxabicyclic series.


1982 ◽  
Vol 60 (8) ◽  
pp. 1030-1033 ◽  
Author(s):  
J. Bryan Jones ◽  
Harold M. Schwartz

The effects have been evaluated of up to 50% (v/v) of methanol, tert-butyl alcohol, dimethylsulfoxide, sulfolane, acetonitrile, dimethylformamide, N-methyl-2-pyrrolidone, hexamethylphosphoramide, acetone, 2-butanone, tetrahydrofuran, dimethoxyethane, diglyme, and dioxane on horse liver alcohol dehydrogenase (HLADH)-catalyzed oxidation of the representative alcohol substrate cyclohexanol. With the exception of dimethylsulfoxide and dimethylformamide, all solvents tested are suitable for use as cosolvents with HLADH in the oxidative and reductive directions.


Sign in / Sign up

Export Citation Format

Share Document