Transition-metal-free and organic solvent-free conversion of N-substituted 2-aminobiaryls into corresponding carbazoles via intramolecular oxidative radical cyclization induced by peroxodisulfate

被引:31
|
作者
Natarajan, Palani [1 ]
Priya
Chuskit, Deachen
机构
[1] Panjab Univ, Dept Chem, Chandigarh 160014, India
关键词
C-H AMINATION; VISIBLE-LIGHT PHOTOREDOX; DIELS-ALDER REACTION; BOND FORMATION; BIOLOGICAL EVALUATION; ACTIVATED PERSULFATE; AMBIENT-TEMPERATURE; CATALYZED SYNTHESIS; MURRAYA-KOENIGII; ANTITUMOR AGENTS;
D O I
10.1039/c7gc03130k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An atom-economical and environmentally benign approach for the synthesis of N-substituted carbazoles from analogous 2-aminobiaryls using peroxodisulfate in water is reported. The reactions proceeded through an intramolecular oxidative radical cyclization of N-substituted 2-aminobiaryls with in situ reoxidation of the resulting radical species. When compared to known methods for the synthesis of N-substituted carbazoles from 2-amidobiaryls, this protocol is practical, efficient and does not require a transition metal catalyst or toxic organic solvents.
引用
收藏
页码:5854 / 5861
页数:8
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