化学
烷基化
激进的
催化循环
金属
催化作用
烷基
配体(生物化学)
氯
药物化学
电子转移
光化学
有机化学
生物化学
受体
作者
Tomislav Rovis,Yi Cheng Kang,Sean M. Treacy
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2021-08-09
卷期号:32 (17): 1767-1771
被引量:34
标识
DOI:10.1055/s-0040-1720388
摘要
Abstract We report the FeCl3-catalyzed alkylation of nonactivated C(sp3)–H bonds. Photoinduced ligand-to-metal charge transfer at the iron center generates chlorine radicals that then preferentially abstract hydrogen atoms from electron-rich C(sp3)–H bonds distal to electron-withdrawing functional groups. The resultant alkyl radicals are trapped by electron-deficient olefins, and the catalytic cycle is closed by Fe(II) recombination and protodemetalation.
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