| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10579805 | Tetrahedron: Asymmetry | 2005 | 8 Pages |
Abstract
Heptakis(2-O-decanoyl)-β-cyclodextrin was synthesised from native β-cyclodextrin and vinyl decanoate in a one-step reaction catalysed by thermolysin in DMSO. The regioselectivity was directed primarily at the C-2 position but depended on the chain length of the acyl donor.
Related Topics
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Authors
Ninfa Rangel Pedersen, Janni Brogaard Kristensen, Guy Bauw, Bart Jan Ravoo, Raphael Darcy, Kim Lambertsen Larsen, Lars Haastrup Pedersen,