Please use this identifier to cite or link to this item:
|Title:||Preparative scale enantioseparation of flurbiprofen by lipase-catalysed reaction||Authors:||Duan, G.
|Issue Date:||1-Dec-1998||Citation:||Duan, G.,Ching, C.B. (1998-12-01). Preparative scale enantioseparation of flurbiprofen by lipase-catalysed reaction. Biochemical Engineering Journal 2 (3) : 237-245. ScholarBank@NUS Repository.||Abstract:||Effects of reaction media, alcohols and water on the enzyme activity of the immobilised Candida antarctica lipase were investigated for the separation of racemic flurbiprofen by an esterification reaction catalysed by immobilised enzyme in organic media. The S-enantiomer of flurbiprofen was directly resolved by the immobilised lipase esterification reaction in acetonitrile. Ping-Pong Bi-Bi kinetics were found to fit the initial reaction well of all the experimental runs. Model parameters for the reaction kinetics were evaluated from experiments at relatively low substrate concentrations, have shown to be applicable for preparative separation scale at high concentrations. Finally, the gram-scale production of single enantiomer with the optical purity of 93% e.e. was obtained. © 1998 Elsevier Science S.A. All rights reserved.||Source Title:||Biochemical Engineering Journal||URI:||http://scholarbank.nus.edu.sg/handle/10635/91652||ISSN:||1369703X|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 16, 2020
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.