An approach for quinolines via palladium-catalyzed Heck coupling followed by cyclization

被引：37

作者：

Cho, Chan Sik ^{[1
]}

Kim, Jun Uk

机构：

[1] Kyungpook Natl Univ, Ind Technol Res Inst, Taegu 702701, South Korea

[2] Kyungpook Natl Univ, Dept Appl Chem, Taegu 702701, South Korea

来源：

TETRAHEDRON LETTERS | 2007年 / 48卷 / 22期

关键词：

alkenes; cyclization; heck reaction; quinolines; quinolones; palladium catalyst;

D O I：

10.1016/j.tetlet.2007.04.001

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

2-Iodoaniline reacts with alpha,beta-unsaturated carbonyl compounds in DMF at 100 degrees C in the presence of a catalytic amount of a palladium catalyst along with a base to afford the corresponding quinolones or quinolines in moderate to good yields. (C) 2007 Elsevier Ltd. All rights reserved.

引用

页码：3775 / 3778

页数：4

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