化学
烷基化
范围(计算机科学)
基质(水族馆)
组合化学
表面改性
反应条件
催化作用
有机化学
协议(科学)
反应性(心理学)
可扩展性
分子
作者
Rui-Qiang Jiao,Jingtai Pei,Zhenguo Xi,Licun Chu,Hongyin Gao
出处
期刊:Organic Letters
[American Chemical Society]
日期:2026-03-12
卷期号:28 (12): 3820-3825
被引量:1
标识
DOI:10.1021/acs.orglett.6c00585
摘要
The direct para -selective functionalization of arenes is difficult under mild conditions without the use of directing groups and transition-metal catalysts. Here we present a fluorosulfuryl imidazolium triflate-mediated direct para -selective C–H arylation and alkylation of N -arylhydroxylamines. This protocol exhibits a broad substrate scope and great functional-group adaptability. Moreover, the potential for scalable production and the feasibility of further modifications of the products showcase the practical utility of this method in synthetic applications.
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