化学
羰基化
一氧化碳
试剂
基质(水族馆)
限制
光化学
溴化物
功能群
组合化学
氢键
反应机理
三键
反应中间体
催化作用
氧化加成
一氧化碳
还原消去
醋酸
氢原子
氢
双键
有机化学
碳原子
碳纤维
反应条件
键裂
密度泛函理论
电子转移
氧化磷酸化
钯
立体化学
化学合成
作者
Ling Li,Chuqian Tang,Guangying Huang,Shengqing Zhu,Yuyang Bai,Lingling Chu
摘要
ABSTRACT We report a visible light‐driven, metallaphotoredox‐catalyzed acceptorless dehydrogenative carbonylation of benzylic C─H bonds with carbon monoxide and nucleophiles. Enabled by a long‐chain diphosphine ligated nickel(II) bromide complex, this protocol uniquely employs C(sp 3 )─H bonds as limiting reagents under ambient temperature and CO atmosphere, affording esters and related carbonyls under oxidant‐free conditions with H 2 as the sole byproduct. The reaction exhibits broad substrate scope, tolerating diverse functional groups and complex bioactive scaffolds. Mechanistic studies are consistent with a pathway involving photoinduced hydrogen atom transfer and nickel‐mediated carbonylation.
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