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Stereoselective esterification of 2,6-dimethyl-1,7-heptanedioic acid, catalysed by Candida rugosa lipase
Mid Sweden University, Faculty of Science, Technology and Media, Department of Natural Sciences.ORCID iD: 0000-0002-5543-2041
Mid Sweden University, Faculty of Science, Technology and Media, Department of Natural Sciences.
Mid Sweden University, Faculty of Science, Technology and Media, Department of Natural Sciences.
Responsible organisation
2003 (English)In: Journal of Molecular Catalysis B: Enzymatic, ISSN 1381-1177, Vol. 23, no 1, 53-59 p.Article in journal (Refereed) Published
Abstract [en]

The immobilised Candida rugosa lipase (CRL) displayed S-preference for both stereogenic centres in this sequential esterification of 2,6-dimethyl-1,7-heptanedioic acid (1) (pure meso and meso: (+/-) mixture, 53/47) with n-butanol in cyclohexane at a(w) = 0.8. The reaction was faster when short-chain primary n-alcohols was used and very slow, or even none reactive, when a Ion-chain alcohol was used.

Place, publisher, year, edition, pages
2003. Vol. 23, no 1, 53-59 p.
Keyword [en]
organic chemistry
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:miun:diva-1962DOI: 10.1016/S1381-1177(03)00067-5ISI: 000184323100008Scopus ID: 0037678457Local ID: 815OAI: oai:DiVA.org:miun-1962DiVA: diva2:26994
Available from: 2008-09-30 Created: 2008-09-30 Last updated: 2016-09-29Bibliographically approved

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Hedenström, ErikEdlund, HelenLund, Susan
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