摘要
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.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 10185-10188 |
| 页数 | 4 |
| 期刊 | Organic and Biomolecular Chemistry |
| 卷 | 14 |
| 期 | 43 |
| DOI | |
| 出版状态 | 已出版 - 2016 |
学术指纹
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