Double enantioselective esterification of racemic acids and alcohols by lipase fromCandida cylindracea
β Scribed by Pei-Yeh Chen; Shih-Hsiung Wu; Kung-Tsung Wang
- Publisher
- Springer Netherlands
- Year
- 1993
- Tongue
- English
- Weight
- 226 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0141-5492
No coin nor oath required. For personal study only.
β¦ Synopsis
Doubly
enantioselective lipase-catalyzed esterification of racemic acids and alcohols was proceeded in n-hexane.
The enantioselectivities of the lipase toward both of racemic substrates were affected reciprocally.
It showed that the active site of the lipase was quite flexible.
π SIMILAR VOLUMES
## Abstract Lipase (EC 3.1.1.3) was immobilized on cellulose acetateβTiO~2~ gel fibre by the solβgel method. The immobilized lipases were used for esterification of __n__βbutyric acid with __n__βbutyl alcohol and enantioselective acylation of (__R, S__)βphenylethanol using vinyl acetate as an acyl