催化作用
合成子
部分
化学
表面改性
激进的
组合化学
光化学
光催化
氢原子
氢键
烷基
基质(水族馆)
合理设计
超分子化学
反应性(心理学)
纳米技术
氢
化学计量学
Atom(片上系统)
有机化学
有机催化
均相催化
原子经济
反应中间体
胺气处理
钯
作者
Boya Feng,Mattia Lepori,Michał Domański,Soňa Boháčová,Daniel Bím,Lucie Ludvíková,Tomáš Slanina,Prakash C. Tiwari,Guodong Zhang,Luigi Dolcini,Timothy Noël,Joshua P. Barham
标识
DOI:10.1038/s41929-026-01539-2
摘要
Abstract The introduction of diverse functionalities into omnipresent aliphatic C–H bonds is of notable value yet challenging in catalysis. While hydrogen atom transfer has emerged as a premier strategy, existing protocols frequently rely on O-centred radicals either generated from hazardous stoichiometric peroxides or within photocatalysts that are promiscuous in their excited state reactivity and non-conducive to structural tuning around the reactive centre. Here we disclose a general platform of readily prepared 9-arylacridine catalysts—a class of neutral, N-centred photocatalysts—that mediate aliphatic C–H bond hydrogen atom transfer under mild conditions. This strategy enables efficient generation of alkyl radicals, allowing various functionalizations ranging from activated substrates to gaseous ethane. The platform features broad substrate scope, scalability and compatibility with transition metal catalysis as well as multicomponent reactions. Its utility is demonstrated in the streamlined synthesis of pharmaceutical synthons and late-stage functionalization of bioactive molecules. Detailed mechanistic studies highlight the crucial role of ortho -substituents on the 9-aryl moiety of catalysts, providing a rational basis for catalyst design.
科研通智能强力驱动
Strongly Powered by AbleSci AI