| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1388516 | Carbohydrate Research | 2008 | 7 Pages |
Abstract
Protected pentofuranose, hexofuranose and hexopyranose hemiacetals were found to react efficiently with amines carrying a deactivating group (alkoxycarbonyl, tosyl or phosphoryl group) in the presence of a Lewis acid to give the corresponding, stable glycosylamines. Such glycosylamine derivatives are useful substrates for further elaboration into nitrogen-containing natural products and carbohydrate mimetics.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Virginie Liautard, Christelle Pillard, Valérie Desvergnes, Olivier R. Martin,