| Title : R-stereopreference analysis of lipase Novozym 435 in kinetic resolution of flurbiprofen - Zhang_2007_Chirality_19_245 |
| Author(s) : Zhang HY , Wang X , Ching CB |
| Ref : Chirality , 19 :245 , 2007 |
|
Abstract :
Immobilized lipase from Candida antarctica (Novozym 435) was employed in the kinetic resolution of racemic flurbiprofen by enantioselective esterification with methanol. It was found that the lipase has the R-stereopreference and the reaction matches Bi Bi Ping Pong mechanism with dead-end inhibition of methanol. Furthermore, the R-stereopreference was analyzed in details from the aspects of enzymatic kinetic mechanism and reaction activation energy of both enantiomers. The R-enantiomer shows lower activation energy and higher maximum reaction rate than the S-enantiomer, which implies the R-stereopreference of the lipase and makes the kinetic resolution of flurbiprofen via enzymatic reaction feasible. |
| PubMedSearch : Zhang_2007_Chirality_19_245 |
| PubMedID: 17094073 |
| Substrate | Ethyl-Flurbiprofen |
Zhang HY, Wang X, Ching CB (2007)
R-stereopreference analysis of lipase Novozym 435 in kinetic resolution of flurbiprofen
Chirality
19 :245
Zhang HY, Wang X, Ching CB (2007)
Chirality
19 :245