## Abstract Sodium bis (2‐ethylhexyl polyoxyethylene) sulfosuccinates, which can be structurally viewed as chemically modified AOT (MAOT), were prepared and successfully used to form reverse micelles in isooctane. The activity and stability of __Candida rugosa__ lipase (glycerol‐ester hydrolase, EC
Enantioselective synthesis of ibuprofen esters in AOT/isooctane microemulsions by Candida cylindracea lipase
✍ Scribed by Gun Hedström; Maria Backlund; J. Peter Slotte
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 659 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0006-3592
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The lipase-catalyzed enantioselective esterification of ibuprofen has been studied in a media, composed only of substrates. When racemic ibuprofen is used, the alcohol-chain length affects the esterification rates of individual enantiomers, but it does not affect the enantioselectivity. Water activi
## Abstract __Candida rugosa__ lipases (CRLs) were immobilised by adsorption onto a commercial polypropylene powder EP100™. Two commercial CRLs from Sigma and Amano were used together with two CRLs obtained by fed‐batch fermentation using oleic acid as a carbon source (UAB‐CRL). Significant differe
## Abstract The effect of solvents and solvent mixtures on the synthesis of myristic acid esters of different carbohydrates with an immobilized lipase from __C. antarctica__ was investigated. The rate of myristyl glucose synthesized by the enzyme was increased from 3.7 to 20.2 μmol min^−1^ g^−1^ by