区域选择性
催化作用
催化循环
镍
化学
齿合度
组合化学
功能群
有机化学
晶体结构
聚合物
作者
Shenghao Wang,Chun Luo,Lei Zhao,Junsong Zhao,Lanlan Zhang,Bolin Zhu,Chao Wang
标识
DOI:10.1016/j.xcrp.2021.100574
摘要
Catalytic difunctionalization of alkenes has been a prominent research theme in recent years. Here, we develop a removable bidentate picolinamide-assisted regioselective dicarbofunctionalization of homoallylic amines with organohalides and arylboronic acids. The catalytic system, using cost-effective and air-stable Ni(II) precatalyst, which could be activated by arylboronic acids, provides access to the regioselective diarylation and arylalkylation of unactivated alkenes. This reaction is compatible with α- or β-substituted terminal alkenes and internal alkenes and exhibits excellent functional group and heterocycle tolerance. Preliminary mechanistic studies suggest that the reaction proceeds via a NiI/NiIII catalytic cycle rather than a Ni0/NiII cycle. Notably, the general and practical protocol developed herein represents, to the best of our knowledge, the first example of Ni-catalyzed 3-component 2,1-diarylation and arylalkylation of alkenes with arylboronic acids and organohalides.
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