SYNTHESIS OF QUINOLINES VIA INTRAMOLECULAR CYCLIZATION OF BENZYLACETONE OXIME DERIVATIVES CATALYZED WITH TETRABUTYLAMMONIUM PERRHENATE(VII) AND TRIFLUOROMETHANESULFONIC ACID

被引：32

作者：

KUSAMA, H ^{[1
]}

YAMASHITA, Y ^{[1
]}

NARASAKA, K ^{[1
]}

机构：

[1] UNIV TOKYO, GRAD SCH SCI, DEPT CHEM, BUNKYO KU, TOKYO 113, JAPAN

来源：

CHEMISTRY LETTERS | 1995年 / 01期

关键词：

D O I：

10.1246/cl.1995.5

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Intramolecular cyclization reaction on the nitrogen atom of benzylacetone oxime derivatives, which have electron donating group(s) on the phenyl group, proceeds by treatment with tetrabutylammonium perrhenate, trifluoromethanesulfonic acid, and 4-chloranil in refluxing 1,2-dichloroethane to afford quinoline derivatives in good yield.

引用

页码：5 / 6

页数：2

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