摘要
Polysubstituted amidines, benzimidazoles and pyrimidines were synthesized via the electrophilic activation of amides with trifluoromethanesulfonic anhydride and 2-chloropyridine. The one-pot protocol is concise and efficient and the substrates are readily available.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1208-1214 |
| 页数 | 7 |
| 期刊 | Tetrahedron |
| 卷 | 66 |
| 期 | 6 |
| DOI | |
| 出版状态 | 已出版 - 6 2月 2010 |
| 已对外发布 | 是 |
学术指纹
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