胺化
基质(水族馆)
配体(生物化学)
催化循环
芳基
催化作用
偶联反应
光化学
化学
功能群
甲烷氧化偶联
有机合成
组合化学
有机化学
生物化学
海洋学
受体
烷基
聚合物
地质学
作者
Geyang Song,Qi Li,Jiameng Song,Ding‐Zhan Nong,Jianyang Dong,Gang Li,Juan Fan,Chao Wang,Dong Xue
标识
DOI:10.1021/acscatal.4c00788
摘要
Iron-catalyzed cross-coupling reactions are difficult to achieve because they usually require a highly reactive, low-valent iron catalyst to undergo the oxidative addition process. Here, we report a method for light-promoted iron-catalyzed C–N coupling reactions between aryl bromides and amines in the presence of a catalytic amount of a bipyridine ligand under irradiation at 390–395 nm. This method, which does not require external photosensitizers, features a broad substrate scope (70 examples) and good functional group tolerance, providing a platform for the development of iron-catalyzed coupling reactions in organic synthesis. Mechanistic studies indicate that an organic base and light are crucial for the generation of an Fe(I) species and that the reaction involves an Fe(I)/Fe(III) catalytic cycle.
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