镍
烯烃
催化作用
烷基
磺酰
试剂
化学
化学计量学
光催化
功能群
组合化学
光化学
有机化学
光催化
聚合物
作者
Andrés García‐Domínguez,Rahul Mondal,Cristina Nevado
标识
DOI:10.1002/anie.201906692
摘要
Abstract The potential of merging photoredox and nickel catalysis to perform multicomponent alkene difunctionalizations under visible‐light irradiation is demonstrated here. Secondary and tertiary alkyl groups, as well as sulfonyl moieties can be added to the terminal position of the double bond with simultaneous arylation of the internal carbon atom in a single step under mild reaction conditions. The process, devoid of stoichiometric additives, benefits from the use of bench‐stable and easy‐to‐handle reagents, is operationally simple, and tolerates a wide variety of functional groups.
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