Iron-Catalyzed Tandem Reactions of Aldehydes, Terminal Alkynes, and Primary Amines as a Strategy for the Synthesis of Quinoline Derivatives

被引：48

作者：

Zhang, Yicheng ^{[1
]}

Li, Pinhua ^{[1
]}

Wang, Lei ^{[1
,2
]}

机构：

[1] Huaibei Normal Univ, Dept Chem, Huaibei 235000, Anhui, Peoples R China

[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 2011年 / 48卷 / 01期

基金：

中国国家自然科学基金;

关键词：

C-C BOND; SULFIDE OXIDATION; HYDROGEN-PEROXIDE; CROSS-COUPLINGS; EFFICIENT; QUINAZOLINE; HYDROSILYLATION; ARYLATION;

D O I：

10.1002/jhet.417

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

FeCl3-catalyzed three-component tandem condensation/addition/cyclization/oxidation reactions of aldehydes, terminal alkynes, and primary amines have been developed. The processes can provide a diverse range of quinoline derivatives in good yields from simple starting materials. A possible reaction mechanism was proposed.

引用

页码：153 / 157

页数：5

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