| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278711 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
Trichlorosulfonamides undergo reaction with CuCl/amines to furnish either reduced dichlorosulfonamides or amides via a 1,4-aryl shift with loss of SO2 depending upon the reaction conditions. Along with amide hydrolysis these reactions may compete when carrying out relatively slow atom transfer radical cyclisation reactions.
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Physical Sciences and Engineering
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Organic Chemistry
Authors
Andrew J. Clark, Stuart R. Coles, Alana Collis, Thomas Debure, Collette Guy, Nicholas P. Murphy, Paul Wilson,