| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279355 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
1,4-Disubstituted 1,2,3-triazoles containing a pentafluorosulfanylalkyl group were synthesized in good to excellent yields (57-91%) by the click cycloadditions of in situ generated SF5-alkyl azides with aromatic and aliphatic alkynes. Nucleophilic substitution of the SF5 group was observed for the first time in a bench-top reaction.
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Authors
Yangen Huang, Gary L. Gard, Jean'ne M. Shreeve,