化学
废止
区域选择性
钯
分子间力
催化作用
原子经济
甲烷氧化偶联
组合化学
铜
氧化磷酸化
基质(水族馆)
药物化学
光化学
有机化学
分子
生物化学
海洋学
地质学
作者
Yihan Wang,Beining Yang,Bo Wang,Yinyin Li,Zhiying Zhang,Yatang Wang,Wei Guo,Zhiyong Tan,Lvyin Zheng
标识
DOI:10.1021/acs.joc.3c02816
摘要
A palladium-catalyzed intermolecular [2 + 2 + 2] oxidative coupling–annulation of terminal alkenes and alkynes using copper(II) as the oxidant has been developed through direct C–C bond formation. These reactions provide effective access to multiaryl-substituted benzenes with high regioselectivity in the absence of any ligands. The features of this protocol are broad substrate scope, and high atom and step economy. The aggregation-induced emission properties of selected products were further investigated. These synthesized multiaryl-substituted benzenes may be worth exploring for further applications in the fields of advanced functional materials or drugs.
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