| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273530 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
In the presence of triflic anhydride, sulfonylation of arenes with sulfonamides proceeded smoothly in Cl2CHCHCl2 at 80-140 °C, which gave rise to the desired products in good to excellent yields.
Graphical abstractIn the presence of triflic anhydride, sulfonylation of arenes with sulfonamides proceeded smoothly in Cl2CHCHCl2 at 80-140 °C, which gave rise to the desired products in good to excellent yields.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bangben Yao, Yuhong Zhang,