化学
胺化
催化作用
烷基
卤素
区域选择性
基质(水族馆)
芳基
药物化学
卤化物
铜
组合化学
有机化学
海洋学
地质学
作者
Xin‐Yang Lv,Rubén Martı́n
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-05-17
卷期号:25 (20): 3750-3754
被引量:9
标识
DOI:10.1021/acs.orglett.3c01216
摘要
Herein, we describe the development of a copper-catalyzed C(sp3) amination of unactivated secondary alkyl iodides mediated by diaryliodonium salts. Our protocol is enabled by the intermediacy of aryl radical species that undergo halogen atom transfer prior to interfacing with copper catalysts, thus setting the basis for a C–N bond formation at sp3-hybridized carbons. The method is characterized by its mild reaction conditions, excellent regioselectivity, and wide substrate scope.
科研通智能强力驱动
Strongly Powered by AbleSci AI