摘要
An efficient synthesis of 2-substituted quinolines from readily available cyclopropanols and imidamides has been developed, where the cyclopropanol acts as a C3 synthon. With the assistance of a bifunctional imidamide directing group, the reaction occurred via sequential C–H/C–C cleavage and C–C/C–N bond formation. (Figure presented.).
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1620-1625 |
| 页数 | 6 |
| 期刊 | Advanced Synthesis and Catalysis |
| 卷 | 359 |
| 期 | 10 |
| DOI | |
| 出版状态 | 已出版 - 17 5月 2017 |
学术指纹
探究 'Synthesis of 2-Substituted Quinolines via Rhodium(III)-Catalyzed C–H Activation of Imidamides and Coupling with Cyclopropanols' 的科研主题。它们共同构成独一无二的指纹。引用此
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