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Published on: July 30, 2017
Catalytic alkylation of unactivated C(sp3)-H bonds for C(sp3)-C(sp3) bond formation
Zhen Chen1, Meng-Yu Rong, Jing Nie
1Department of Chemistry, Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Tianjin University, and Collaborative Innovation Centre of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. China. majun_an68@tju.edu.cn.
Abstract:
The construction of carbon-carbon bonds is a central tenet of modern synthetic chemistry. Metal-catalyzed C-H functionalization can serve as a particularly powerful tool for achieving carbon-carbon bond formation. This review summarizes the early adventures and recent advancements in catalytic transformation of unactivated C(sp3)-H bonds into C(sp3)-C(sp3) bonds. To date, three main strategies have emerged to enable this transformation, namely, metallocarbene-triggered C(sp3)-H alkylation, auxiliary-directed C(sp3)-H alkylation, and photo-induced C(sp3)-H alkylation. Compared with traditional cross-coupling reactions having both coupling partners activated with functional groups or base-promoted enolate chemistry, catalytic alkylation of unactivated C(sp3)-H bonds for C(sp3)-C(sp3) bond formation not only offers novel disconnections in retrosynthetic analysis, but also represents the future trend in green and atom-economic chemistry.
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