化学
烯丙基重排
烷基化
催化作用
筑地反应
阳离子聚合
立体选择性
组合化学
铑
药物化学
立体化学
有机化学
作者
Ji Yang,Changjun Chen,Haoqiang Zhao,Bohan Li,Zhenni He,Lijin Xu,Qian Shi
标识
DOI:10.1002/adsc.202300074
摘要
Abstract Rh(III)‐catalyzed chelation‐assisted C8‐selective C−H alkenylation and alkylation of 1,2,3,4‐tretrahydroquinolines with styrenes and allylic alcohols have been realized. The cationic Rh(III) catalytic system in combination with a catalytic amount of copper acetate uses oxygen as the terminal oxidant and catalyzes the stereoselective C8‐alkenylation of 1,2,3,4‐tetrahydroquinolines with styrenes to give the corresponding products in 56–93% yields with wide substrate scope and broad functional group compatibility. The reaction can be scaled up. Moreover, this protocol can be extended to the C8‐alkylation of 1,2,3,4‐tetrahydroquinolines with allylic alcohols, providing access to various 8‐(3‐oxoalkyl)‐1,2,3,4‐tetrahydroquinolines in 77–90% yields. The selection of N‐directing group is essential for catalysis, and the readily installable and removable N‐(2‐pyrimidyl) group proves to be optimal choice. Preliminary mechanistic studies are performed to gain insights into the reaction mechanism. magnified image
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