Abstract
By using a diaryliodonium salt as a benzyne precursor, a transition metal-free approach for N-arylation of secondary amides is developed. This novel benzyne precursor, which can be prepared easily by a one step process from an aryl iodide, shows different reactivities with previous benzyne precursors in the N-arylation reaction. Mechanistic studies confirm the involvement of benzyne species (generated in situ from the diaryliodonium salts) as key intermediates.
| Original language | English |
|---|---|
| Pages (from-to) | 10185-10188 |
| Number of pages | 4 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 14 |
| Issue number | 43 |
| DOIs | |
| State | Published - 2016 |
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