Iron(III)-Catalyzed Ortho-Preferred Radical Nucleophilic Alkylation of Electron-Deficient Arenes

被引:22
|
作者
Yu, Fei [1 ]
Wang, Ting [2 ]
Zhou, Huan [1 ]
Li, Yajun [1 ]
Zhang, Xinhao [2 ]
Bao, Hongli [1 ]
机构
[1] Univ Chinese Acad Sci, Key Lab Coal Ethylene Glycol & Its Related Techno, State Key Lab Struct Chem, Fujian Inst Res Struct Matter, 155 Yangqiao Rd West, Fuzhou 350002, Fujian, Peoples R China
[2] Peking Univ, Shenzhen Grad Sch, Key Lab Chem Genom, Lab Computat Chem & Drug Design, Shenzhen 518055, Peoples R China
关键词
FRIEDEL-CRAFTS ALKYLATION; C-H PERFLUOROALKYLATION; ORGANIC-SYNTHESIS; ALCOHOLS; FUNCTIONALIZATION; ALLYLATION; BENZENES;
D O I
10.1021/acs.orglett.7b03244
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The untraditional iron-catalyzed, ortho-preferred, radical alkylation of electron-deficient (hetero)arenes is reported. A variety of electron-deficient arenes were shown to react with various primary alkyl sources, producing the alkylated (hetero)arenes in good yields. This reaction might be an alkyl radical, nucleophilic aromatic substitution reaction, rather than the traditional electrophilic Friedel-Crafts reaction. HOMO-LUMO analysis and DFT studies on the key transition states underlying the regioselectivity are consistent with the observed reactions and the conclusions.
引用
收藏
页码:6538 / 6541
页数:4
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