Tsuzuki Saori, Sakurai Shunya, Matsumoto Akira, Kano Taichi, Maruoka Keiji
Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo, Kyoto 606-8501, Japan.
Chem Commun (Camb). 2021 Aug 10;57(64):7942-7945. doi: 10.1039/d1cc02983e.
A Ni-catalyzed direct C-H alkylation of N-quinolylbenzamides using alkylsilyl peroxides as alkyl-radical precursors is described. The reaction forms a new C(sp3)-C(sp2) bond via the selective cleavage of both C(sp3)-C(sp3) and C(sp2)-H bonds. This transformation shows a high functional-group tolerance and, due to the structural diversity of alkylsilyl peroxides, a wide range of alkyl chains including functional groups and complex structures can be introduced at the ortho-position of readily available N-quinolylbenzamide derivatives. Mechanistic studies suggest that the reaction involves a radical mechanism.
描述了一种使用烷基硅基过氧化物作为烷基自由基前体的镍催化的N-喹啉基苯甲酰胺的直接C-H烷基化反应。该反应通过选择性裂解C(sp3)-C(sp3)键和C(sp2)-H键形成新的C(sp3)-C(sp2)键。这种转化表现出高官能团耐受性,并且由于烷基硅基过氧化物的结构多样性,可以在容易获得的N-喹啉基苯甲酰胺衍生物的邻位引入包括官能团和复杂结构的各种烷基链。机理研究表明该反应涉及自由基机理。