Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267418 | Tetrahedron Letters | 2012 | 6 Pages |
Abstract
We have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles through a Cu(I)-promoted azide-alkyne 1,3-dipolar cycloaddition between a TMS-protected C-alkynyl-glycoside and organic azides. The reaction was accelerated by ultrasound irradiation and the addition of a base was not necessary to obtain the 1,2,3-triazole product. Moreover, further manipulation of the products led to chiral molecules with a C-glycoside linkage.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hélio A. Stefani, Nathália C.S. Silva, Flávia Manarin, Diogo S. Lüdtke, Julio Zukerman-Schpector, Lucas Sousa Madureira, Edward R.T. Tiekink,