| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277228 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The efficient synthesis of d-rhamnoside and the corresponding methods for its regioselective protections and deprotections have been developed in order to provide key building blocks for complex oligosaccharide syntheses toward vaccines against bacterial infections.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Régis Fauré, Tze Chieh Shiao, Sonia Damerval, René Roy,