| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278325 | Tetrahedron Letters | 2011 | 6 Pages |
Abstract
Starting from suitably protected 3- and 4-aminobenzenesulfonamides, a practical two-step strategy for the synthesis of unsubstituted N-aryl and heteroarylaminobenzenesulfonamides was devised. Strong bases are tolerated during the N-arylation step. Overall moderate to excellent yields are reported.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Franck Lach, Marie-Jeanne Pasquet, Mylène Chabanne,