Immobilization does not influence the enantioselectivity of CAL-B catalyzed kinetic resolution of secondary alcohols
Decreasing 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 enzym...
Published in: | Tetrahedron: Asymmetry |
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Main Authors: | , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Elsevier
2005
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Subjects: | |
Online Access: | http://hdl.handle.net/11250/2432641 https://doi.org/10.1016/j.tetasy.2004.11.081 |
Summary: | Decreasing 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. Author preprint. © 2004 Elsevier Ltd. All rights reserved |
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