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
收藏
页码：153 / 157
页数：5
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