Effect of solvent structure on enantioselectivity of lipase-catalyzed transesterification
β Scribed by Kaoru Nakamura; Yasushi Takebe; Takashi Kitayama; Atsuyoshi Ohno
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 152 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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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
The effect of the acyl group of acylating agents on the enantioselectivity in the lipasecatalyzed transesterifications of racemie 2-[(N,N-dimethylearbamoyl)methyl]-3-eyelopenten-l-ol in diisopropyl ether was found 1o be significant. The enantioselectivity was enhanced markedly by changing the aeylat
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