Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1388546 | Carbohydrate Research | 2010 | 6 Pages |
Abstract
The solid-phase synthesis of methyl 2-deoxy-3-O-benzyl-d,l-arabino-hexopyranoside was achieved in a six-step sequence via a de novo strategy based on the hetero-Diels–Alder reaction of a vinyl ether supported on an azalactone-functionalized polystyrene resin, followed by the functional modification of the heteroadduct and the final release of the methyl glycoside by acidic solvolysis.
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Related Topics
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Organic Chemistry
Authors
Céline Lucchesi, Amélie Arboré, Sagrario Pascual, Laurent Fontaine, Christian Maignan, Gilles Dujardin,