Substituent effects on the enantioselectivity for the lipase-catalyzed esterifications in organic solvents were studied by use of 2-(4-substituted phenoxy)propionic acids as the substrates with various substituents of H, F, Cl, CF 3 , CH 3 , CH 3 CH 2 , and CH 3 O. The distinction in the behavior of
Effect of temperature on lipase-catalyzed esterification in organic solvent
β Scribed by Yoshitaka Yasufuku; Shin-ichi Ueji
- Publisher
- Springer Netherlands
- Year
- 1995
- Tongue
- English
- Weight
- 254 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0141-5492
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β¦ Synopsis
For the esterification of 2-(4-ethylphenoxy)propionic acid catalyzed by lipase MY (Candida rugosa) in isopropyl ether containing a suitable amount of water, the enantioselectivity for the reaction has become higher asthe reaction temperature increasing.
In contrast, the reverse trend of the temperature effect has been observed for lipase AY (Candida rugosa). A model for these temperature dependence has been proposed.
π SIMILAR VOLUMES
Lipase-catalyzed transesterifications of cis-and Iran.+4-methylcyclohexanols with vinyl acetate in various organic solvents have been studied, and the cffcct of' solvent on activity and stereoselectivity of lipase has been investigated. Initial rate of the reaction increases with the increase in hyd