催化作用
基质(水族馆)
材料科学
化学
组合化学
纳米技术
化学工程
群(周期表)
密度泛函理论
自然(考古学)
结晶学
立体化学
作者
Jun Hu,Suman Pradhan,Yuman Qin,Wenhao Su,Peng Ren,Lindsey Frederiksen,Susanna Monti,Giovanni Bacaro,Aleksander Jaworski,Anna Rokicińska,Kaan Karaca,Piotr Kuśtrowski,Gianvito Vilé,David Reyes,Paul J. Dyson,Shoubhik Das
标识
DOI:10.1002/anie.202524517
摘要
ABSTRACT Direct functionalization of aromatic C─H bonds is crucial in organic synthesis due to their wide applications in pharmaceutical chemistry and materials engineering, yet precise site selectivity remains challenging. Traditional methods often rely on electrophilic aromatic substitution or transition metal catalysis with directing group strategies, which can result in product mixtures or require pre‐installed functional groups. In this respect, recent advances using single‐atom catalysts (SACs) are promising due to their enhanced reactivity and selectivity. This study introduces a robust catalytic system for undirected para ‐C─H functionalization of electron‐rich arenes by using an atomically dispersed copper‐based photocatalyst. The method bypasses the requirement of pre‐installed directing groups, achieving site‐selective functionalization through an η 2 interaction with arenes under mild conditions, with a broad substrate scope, and excellent catalyst recyclability. Furthermore, this approach offers a novel method for incorporating functional groups into complex drug molecules, which is crucial in the synthesis of pharmaceuticals and natural products.
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