催化作用
硝基苯
反应性(心理学)
化学
功能群
光化学
基质(水族馆)
光敏剂
组合化学
反应条件
激进的
有机化学
替代医学
聚合物
病理
地质学
海洋学
医学
作者
Jingjing Tang,Xiaoqiang Yu,Yoshinori Yamamoto,Ming Bao
出处
期刊:ACS Catalysis
日期:2021-11-03
卷期号:11 (22): 13955-13961
被引量:30
标识
DOI:10.1021/acscatal.1c04538
摘要
A visible-light-promoted and simple iron salt-catalyzed N-arylation was achieved efficiently under external photosensitizer-free conditions. Arylboronic acids and bench-stable dioxazolones were used for this cross-coupling reaction. This reaction features high reactivity, wide substrate scope, good functional group tolerance, simple operation procedure, and mild reaction conditions. Preliminary mechanistic investigations were conducted to support a radical pathway. This method may contribute to shift the paradigm of iron-catalyzed C–N bond construction and nitrene transfer chemistry.
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