烯丙基重排
羰基化
催化作用
镍
化学
酒
偶联反应
组合化学
烯丙醇
表面改性
有机化学
一氧化碳
物理化学
作者
Chenglong Wang,Xianqing Wu,Haiyan Li,Jingping Qü,Yifeng Chen
标识
DOI:10.1002/ange.202210484
摘要
Abstract A nickel‐catalyzed three‐component carbonylative cross‐coupling reaction of allylic alcohols and organoalanes with CO at atmospheric pressure is reported, enabling the expedient formation of β,γ‐unsaturated ketones with broad scope. Particularly, the chemoselective allylic carbonylation of diols further highlights the practicability of this protocol. The leverage of organoalanes as both the coupling components and the activators for the alcohol functionalization is crucial for this method, thus no extraneous activators are required.
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