| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281471 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
A direct coupling of aryl donor and tetra-O-acetylribose in the presence of Lewis acid led to β-C-nucleosides in good yields. In contrast, for deactivated electron-poor aromatics, a modified Vorbrüggen ribosylation reaction was investigated and successfully applied in the case of 2-trimethylsilyl-thiazole.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marie Spadafora, Mohamed Mehiri, Alain Burger, Rachid Benhida,