Kinetics and Validation of Mathematical Models of Enantioselective Transesterification in Organic Solvents
- 1 January 1992
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- The Kinetics of Transesterification by α-Chymotrypsin of a Racemic Mixture of Phenylalanine Propyl Ester with 1,4-ButanediolBiocatalysis, 1992
- Transesterification of Phenylalanine by Means of Chymotrypsin in the Presence of DimethylsulfoxideBiocatalysis, 1992
- Mathematical Modelling of Lipase Catalysed Resolution ofO-Acetyl andO-Formyl Derivatives of Secondary AlcoholsBiocatalysis, 1991
- Lipase-catalyzed irreversible transesterification using enol esters: resolution of prostaglandin synthons 4-hydroxy-2-alkyl-2-cyclopentenones and inversion of the 4S enantiomer to the 4R enantiomerThe Journal of Organic Chemistry, 1990
- Screening and Application of Microbial Esterases for the Enantioselective Synthesis of Chiral Glycerol DerivativesBiocatalysis, 1990
- Enzyme-catalyzed asymmetric synthesis. 8. Enantioselectivity of pig liver esterase catalyzed hydrolyses of 4-substituted meso cyclopentane 1,2-diestersThe Journal of Organic Chemistry, 1989
- Enzymatic Separation and Resolution of Nucleophiles: A Predictive Kinetic ModelBiocatalysis, 1988
- Lipase-catalyzed reactions in organic media: competition and applicationsBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
- Application of microbes and microbial esterases to the preparation of optically active N-acetylindoline-2-carboxylic acid.Agricultural and Biological Chemistry, 1987
- Aspects Of Biocatalyst Stability In Organic SolventsBiocatalysis, 1987