Silver-mediated radical aryltrifluoromethylthiolation of activated alkenes by S-trifluoromethyl 4-methylbenzenesulfonothioate |
| |
Authors: | Xia Zhao Bo Yang Aoqi Wei Jianqiao Sheng Miaomiao Tian Quan Li Kui Lu |
| |
Institution: | 1. College of Chemistry, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, Key laboratory of Inorganic-organic Hybrid Functional Material Chemistry, Ministry of Education, Tianjin Normal University, Tianjin 300387, China;2. College of Biotechnology, Tianjin University of Science & Technology, Tianjin 300457, China |
| |
Abstract: | Herein, we describe the preparation of trifluoromethylthiol-substituted oxindoles by silver-mediated aryltrifluoromethylthiolation of activated alkenes, using S-trifluoromethyl 4-methylbenzenesulfonothioate as a F3CS radical source and showing that the reagent availability, mild conditions, and broad functional group compatibility of this transformation make it a viable alternative strategy of constructing Csp3![/>SCF<sub>3</sub> bonds.</td>
</tr>
<tr>
<td align=](https://sdfestaticassets-us-east-1.sciencedirectassets.com/prod/dfcf6ffc10ef1f214ae15002a0bf0d0980d00cf9/entities/sbnd) | |
Keywords: | Silver-mediated Radical Aryltrifluoromethylthiolation Activated alkenes Oxindole |
本文献已被 ScienceDirect 等数据库收录! |
|