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dc.contributor.authorJacobsen, Elisabeth Egholm
dc.contributor.authorAndresen, Liv Siri
dc.contributor.authorAnthonsen, Thorleif
dc.date.accessioned2017-03-02T08:30:27Z
dc.date.available2017-03-02T08:30:27Z
dc.date.created2006-01-02T14:31:54Z
dc.date.issued2005
dc.identifier.citationTetrahedron: asymmetry. 2005, 16 847-850.nb_NO
dc.identifier.issn0957-4166
dc.identifier.urihttp://hdl.handle.net/11250/2432641
dc.description.abstractDecreasing enantioselectivity (E-value) by conversion has been observed in transesterification reactions of secondary alcohols catalyzed by a pure protein formulation of lipase B from Candida antarctica (Novozym 525 F). Addition of a range of enantiopure alcohols caused a temporary increase in enzyme selectivity in the transesterification reaction of 3-chloro-1-phenoxy-2-propanol with vinyl butanoate.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleImmobilization does not influence the enantioselectivity of CAL-B catalyzed kinetic resolution of secondary alcoholsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.source.pagenumber847-850nb_NO
dc.source.volume16nb_NO
dc.source.journalTetrahedron: asymmetrynb_NO
dc.identifier.doihttp://dx.doi.org/10.1016/j.tetasy.2004.11.081
dc.identifier.cristin397697
dc.description.localcodeAuthor preprint. © 2004 Elsevier Ltd. All rights reservednb_NO
cristin.unitcode194,66,25,0
cristin.unitnameInstitutt for kjemi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextpreprint
cristin.qualitycode1


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