Palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines with isocyanides through double sp2 C-H bonds cleavage: facile synthesis of 4-aminoquinoline derivatives

被引：25
|
作者：
Zheng, Qiang [1 ,2 ]
Luo, Puying [3 ]
Lin, Yuqing [1 ,2 ]
Chen, Wenfan [1 ,2 ]
Liu, Xiuxiu [1 ,2 ]
Zhang, Yadong [1 ,2 ]
Ding, Qiuping [1 ,2 ]
机构：
[1] Jiangxi Normal Univ, Minist Educ, Key Lab Funct Small Organ Mol, Nanchang 330022, Jiangxi, Peoples R China
[2] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
[3] Jiangxi Prov Peoples Hosp, Dept Obstet & Gynecol, Nanchang 330006, Jiangxi, Peoples R China
来源：
ORGANIC & BIOMOLECULAR CHEMISTRY | 2015年 / 13卷 / 16期
基金：
中国博士后科学基金; 中国国家自然科学基金;
关键词：
ONE-POT SYNTHESIS; QUINOLINE DERIVATIVES; VERSATILE SYNTHESIS; EFFICIENT SYNTHESIS; ANTI-HIV-1; AGENTS; CASCADE REACTIONS; INSERTION; ACTIVATION; PYRROLES; INDOLES;
D O I：
10.1039/c5ob00329f
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An efficient method for the synthesis of 4-aminoquinolines via palladium-catalyzed intermolecular oxidative cyclization of N-aryl enamines and isocyanides through double sp(2) C-H bonds cleavage has been developed.
引用
收藏
页码：4657 / 4660
页数：4
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