121961-00-0Relevant articles and documents
Pig liver acetone powder (PLAP) as biocatalyst: Enantioselective synthesis of trans-2-alkoxycyclohexan-1-ols
Basavaiah, Deevi,Krishna, Peddinti Rama
, p. 10521 - 10530 (1994)
Pig liver acetone powder (PLAP) enantioselectively hydrolyzes trans-1- acetoxy-2-alkoxycyclohexanes 1a-6a in biphasic medium (ether and phosphate buffer) to provide the required (1R,2R)-2-alkoxycyclohexan-1-ols in 61-82% enantiomeric purities.
Enantiomerically Pure Cyclohexanols and Cyclohexane-1,2-Diol Derivatives; Chiral Auxiliaries and Substitutes for (-)-8-Phenylmenthol. A Facile Enzymatic Route
Laumen, Kurt,Breitgoff, Detlef,Seemayer, Robert,Schneider, Manfred P.
, p. 148 - 150 (2007/10/02)
A number of optically active cyclohexanol and cyclohexane-1,2-diol derivatives, chiral auxiliaries and substitutes for (-)- and (+)-8-phenylmenthol, have been prepared by enzymatic hydrolysis of their racemic acetates and chloroacetates in the presence of a highly selective ester hydrolase from Pseudomonas sp. (SAM-II).