异构化
钯
催化作用
化学
芳基
分子内力
苯胺
烯烃
羰基化
光化学
组合化学
药物化学
有机化学
一氧化碳
烷基
作者
Xian‐Jin Zou,Zhao‐Xing Jin,Huiyi Yang,Fei Wu,Zhi‐Hui Ren,Zheng‐Hui Guan
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-04-15
卷期号:63 (26): e202406226-e202406226
被引量:20
标识
DOI:10.1002/anie.202406226
摘要
Abstract In contrast to the kinetically favored outward isomerization‐hydrocarbonylation of alkenes, the disfavored inward isomerization‐hydrocarbonylation of alkenes remains an important challenge. Herein, we have developed a novel and effective palladium‐catalyzed inward isomerization‐hydroaminocarbonylation of unactivated alkenes and aniline hydrochlorides for the formation of synthetically valuable α‐aryl carboxylic amides in high yields and high site‐selectivities. The high efficiency of the reaction is attributed to a relay catalysis strategy, in which the Markovnikov‐favored [PdH]‐P t Bu 3 catalyst is responsible for inward isomerization, while the [PdH]‐Ruphos catalyst is responsible for hydroaminocarbonylation of the resulting conjugated aryl alkenes. The reaction exhibits highly functional group tolerance and provides a new method for formal carbonylation of remote C(sp 3 )−H bond.
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