Studies on the Mechanism of Enzyme-Catalyzed Oxidation Reduction Reactions. III. A Characterization of the Mechanism of the Liver Alcohol Dehydrogenase Reaction*

Biochemistry ◽  
1962 ◽  
Vol 1 (1) ◽  
pp. 41-47 ◽  
Author(s):  
R. H. Baker
Keyword(s):  
Alcohol Dehydrogenase ◽  
Reduction Reactions ◽  
Liver Alcohol Dehydrogenase ◽  
Oxidation Reduction ◽  
Dehydrogenase Reaction ◽  
Catalyzed Oxidation

Enzymes in organic synthesis. 32. Stereospecific horse liver alcohol dehydrogenase-catalyzed oxidations of exo- and endo-oxabicyclic meso diols

1984 ◽  
Vol 62 (11) ◽  
pp. 2578-2582 ◽  
Author(s):  
J. Bryan Jones ◽  
Christopher J. Francis
Keyword(s):  
Alcohol Dehydrogenase ◽  
Organic Synthesis ◽  
Horse Liver Alcohol Dehydrogenase ◽  
Preparative Scale ◽  
Enantiomerically Pure ◽  
Liver Alcohol Dehydrogenase ◽  
Horse Liver ◽  
One Step ◽  
Catalyzed Oxidation ◽  
Enzymes In Organic Synthesis

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.

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