Abstract
A mild and efficient method for the synthesis of N-arylsulfonamides in the presence of 10 mol % of CuCl is demonstrated. The reaction proceeds readily at room temperature in an open flask using a variety of sulfonyl azides and boronic acids without any base, ligand, or additive.
Original language | English |
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Pages (from-to) | 338-341 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 16 |
Issue number | 2 |
DOIs | |
State | Published - 2014 |