| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279081 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Microwave activation coupled with Cu(I) catalysis, under solvent-free conditions, was found to dramatically enhance the 1,3-dipolar cycloaddition between azido-2â²-deoxyribose and terminal alkynes. The process is highly efficient and quantitatively affords, in few minutes, the corresponding 4-substituted 1,2,3-triazolyl-nucleosides.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Raja Guezguez, Khalid Bougrin, Khalid El Akri, Rachid Benhida,