Synthesis of 2-Trifluoromethyl Quinoline by the Reaction of Fluorinated Imine with Alkyne Catalyzed by Indium(III) Triflate

被引：22

作者：

Xie, Haibo ^{[1
]}

Zhu, Jiangtao ^{[1
]}

Chen, Zixian ^{[1
,2
]}

Li, Shan ^{[1
]}

Wu, Yongming ^{[1
]}

机构：

[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China

[2] Huazhong Univ Sci & Technol, Dept Chem, Wuhan 430074, Hubei, Peoples R China

来源：

SYNLETT | 2010年 / 17期

基金：

美国国家科学基金会;

关键词：

alkynes; quinolines; indium; Diels-Alder reaction; imines; ONE-POT SYNTHESIS; SUBSTITUTED QUINOLINES; ARYLIMIDOYL RADICALS; AROMATIC ANNELATION; EFFICIENT SYNTHESIS; BRONSTED ACID; DERIVATIVES; CYCLIZATION; CHLORIDES; AMINES;

D O I：

10.1055/s-0030-1258770

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Preparation of 2-trifluoromethyl-4-aryl quinolines from a variety of readily available alkynes and N-aryl trifluoroethylimine has been achieved via indium(III) triflate catalyzed Diels-Alder reactions.

引用

页码：2659 / 2663

页数：5

共 32 条

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