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

页码：768 / 772

页数：5

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