Annulation based on 8-aminoquinoline assisted C-H activation: an emerging tool in N-heterocycle construction

被引：40
|
作者：
Wan, Jie-Ping [1 ]
Li, Yi [1 ]
Liu, Yunyun [1 ]
机构：
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Peoples R China
来源：
ORGANIC CHEMISTRY FRONTIERS | 2016年 / 3卷 / 06期
基金：
中国国家自然科学基金;
关键词：
UNACTIVATED C(SP(3))-H BONDS; INTRAMOLECULAR AMINATION; ALIPHATIC AMIDES; DIRECTING GROUP; AMIDATION; FUNCTIONALIZATION; CARBOXAMIDES; ALKYNYLATION; C(SP(2))-H; BIDENTATE;
D O I：
10.1039/c6qo00077k
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The synthesis of heterocyclic products via C-H activation has won impressive advances as a newly emerging synthetic strategy. Herein, the recent research advances in heterocycle synthesis employing 8-aminoquinoline directed C-H activation, either in the form of direct intramolecular C-H elaboration or domino reactions involving the C-H activation and other transformation-based annulation reactions are highlighted.
引用
收藏
页码：768 / 772
页数：5
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