摘要
The first iron‐catalyzed 1,2‐difunctionalization of styrenes and conjugated alkenes with silanes and either N or C, using an oxidative radical strategy, is described. Employing FeCl\u003csub\u003e2\u003c/sub\u003e and di‐ tert ‐butyl peroxide allows divergent alkene 1,2‐difunctionalizations, including 1,2‐aminosilylation, 1,2‐arylsilylation, and 1,2‐alkylsilylation, which rely on a wide range of nucleophiles, namely, amines, amides, indoles, pyrroles, and 1,3‐dicarbonyls, thus providing a powerful platform for producing diverse silicon‐containing alkanes.
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单位南昌航空大学; 化学生物传感与计量学国家重点实验室