| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1390964 | Carbohydrate Research | 2006 | 9 Pages |
Abstract
α-Glycosyl ureas can be synthesised directly from tetra-O-benzyl glycosyl azides and isocyanates, using a one-pot procedure that is simple and general in scope. The benzyl protecting groups are easily removed from the urea products by catalytic hydrogenation. The synthesised α-glycosyl ureas represent a new class of neo-glycoconjugates with the potential of being resistant towards carbohydrate processing enzymes.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Aldo Bianchi, Davide Ferrario, Anna Bernardi,