Related Experiment Video
Updated: May 13, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Racemization of enantiopure secondary alcohols by Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase
Musa M Musa1, Robert S Phillips, Maris Laivenieks
1Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran, 31261, KSA. musam@kfupm.edu.sa
Abstract:
Controlled racemization of enantiopure phenyl-ring-containing secondary alcohols is achieved in this study using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus (W110A TeSADH) and in the presence of the reduced and oxidized forms of its cofactor nicotinamide-adenine dinucleotide. Racemization of both enantiomers of alcohols accepted by W110A TeSADH, not only with low, but also with reasonably high, enantiomeric discrimination is achieved by this method. Furthermore, the high tolerance of TeSADH to organic solvents allows TeSADH-catalyzed racemization to be conducted in media containing up to 50% (v/v) of organic solvents.
Related Concept Videos
Stereochemical Effects of Enolization
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation
Reactivity of Enols
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:

