Asymmetric Hydrolyses of 1,2-Diacetoxycyclohexanes by the Cultured Suspension Cells of Marchantia polymorpha
- 1 August 1994
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 23 (8) , 1519-1520
- https://doi.org/10.1246/cl.1994.1519
Abstract
The enantioselectivity in the hydrolyses of cis- and trans-1,2-diacetoxycyclohexanes by the cultured suspension cells of Marchantia polymorpha was very high. The acetoxyl groups at the stereogenic center of (R)-configuration were preferentially hydrolyzed.Keywords
This publication has 8 references indexed in Scilit:
- Enantioselective hydrolysis of 2-methylcyclohexanyl acetates with the cultured cells of Marchantia polymorphaTetrahedron: Asymmetry, 1993
- A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosaThe Journal of Organic Chemistry, 1991
- Biotransformation of exogenous substrates by plant cell culturesPhytochemistry, 1990
- Enzyme-mediated enantioface-differentiating hydrolysis of .alpha.-substituted cycloalkanone enol estersJournal of the American Chemical Society, 1990
- Microbially mediated enantioselective ester hydrolyses utilizing Rhizopus nigricans. A new method of assigning the absolute stereochemistry of acyclic 1-arylalkanolsThe Journal of Organic Chemistry, 1983
- Nutrient utilization and requirement under photoheterotrophic growth of Marchantia polymorpha: Improvement of the culture mediumPhysiologia Plantarum, 1980
- Regeneration of the liverwort Marchantia polymorpha L. From protoplasts isolated from cell suspension culturePlant Science Letters, 1979
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969