化学
胺化
烯丙基重排
烯烃纤维
钯
氧化磷酸化
催化作用
有机化学
组合化学
磷化氢
齿合度
小学(天文学)
分子
甲烷氧化偶联
化学合成
反应条件
过渡金属
胺气处理
作者
Jiarui Li,Yangbin Jin,Mingda Li,Yupeng Chen,Wanqing Wu,Huanfeng Jiang
标识
DOI:10.1002/anie.202520265
摘要
Heteroaryl amines are prone to over coordination in the transition metal-catalyzed olefin oxidation reaction system, which hinders the smooth catalytic reaction. Herein, we report a general method for the direct C─N coupling between inactive olefins and primary and secondary heterocyclic aromatic amines under palladium catalysis, which is an important transition that has not yet been revealed. By employing commercially available palladium catalysts, quinone oxidants, and inexpensive monodentate phosphine ligands, the oxidative amination of diverse heteroaryl amines proceeds smoothly, delivering a broad range of allyl heteroaryl amines with excellent regio- and stereoselectivity. Notably, this strategy enables the late-stage modification of challenging biologically relevant molecules such as adenine and adenosine, further highlighting the practicality and synthetic utility of this reaction.
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