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Please use this identifier to cite or link to this item: https://doi.org/10.1023/A:1018420022398
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dc.titleKinetic study of enantioselective esterification of ketoprofen with n-propanol catalysed by an lipase in an organic medium
dc.contributor.authorDuan, G.
dc.contributor.authorChing, C.B.
dc.contributor.authorLim, E.
dc.contributor.authorAng, C.H.
dc.date.accessioned2014-10-09T08:19:12Z
dc.date.available2014-10-09T08:19:12Z
dc.date.issued1997
dc.identifier.citationDuan, G., Ching, C.B., Lim, E., Ang, C.H. (1997). Kinetic study of enantioselective esterification of ketoprofen with n-propanol catalysed by an lipase in an organic medium. Biotechnology Letters 19 (11) : 1051-1055. ScholarBank@NUS Repository. https://doi.org/10.1023/A:1018420022398
dc.identifier.issn01415492
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91531
dc.description.abstractA kinetic study of an immobilised lipase esterification reaction in dipropyl ether for resolution of ketoprofen indicated a Bi Bi Ping Pong mechanism with dead-end inhibition of the alcohol was occurring for both enantiomers and this is was confirmed experimentally. Parameters in the kinetic equation and reaction activation energies for the two enantiomers were determined by non-linear regression.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1023/A:1018420022398
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.description.doi10.1023/A:1018420022398
dc.description.sourcetitleBiotechnology Letters
dc.description.volume19
dc.description.issue11
dc.description.page1051-1055
dc.description.codenBILED
dc.identifier.isiutA1997YE16600001
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