Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9616801 | Journal of Molecular Catalysis B: Enzymatic | 2005 | 6 Pages |
Abstract
The influence of the nature of acyl donors on the regioselectivity of Candida rugosa lipase for the esterification of streptol - a cyclitol derivative - was investigated. Excellent regioselectivity for the formation of 3,7-disubstituted derivatives was observed for vinyl butyrate (100% 3,7-derivative, 68% yield) and vinyl propionate (100% 3,7-derivative, 46% yield) as acyl donors. In contrast, for vinyl methacrylate as acyl donor, a mixture of 71% 3,7-derivative and 29% 1,7-derivative was obtained. Varying the chain length, a certain dependency of regioselectivity on the acyl donor was observed, however, no logical correlation satisfying all cases was found. Mono-substituted streptol derivatives were obtained by employing Novozym 243.
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Authors
Wolfgang Kroutil, Leonhard Hagmann, Traugott C. Schuez, Volker Jungmann, J. Paul Pachlatko,