A convenient method for the synthesis of 3,5,7-trimethoxy-2-phenyl-4-quinolones

被引：20

作者：

Beney, C ^{[1
]}

Hadjeri, M ^{[1
]}

Mariotte, AM ^{[1
]}

Boumendjel, A ^{[1
]}

机构：

[1] UFR Pharm Grenoble, UMR CNRS 5063, Lab Pharmacognosie, Dept Pharmacochim Mol, F-38706 La Tronche, France

来源：

TETRAHEDRON LETTERS | 2000年 / 41卷 / 36期

关键词：

3-methoxyphenylquinolones; synthesis;

D O I：

10.1016/S0040-4039(00)01226-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The synthesis of 2-aryl-3,5,7-trimethoxy-4-quinoiones was accomplished in three steps starting from 3,5-dimethoxyaniline and an aroyl chloride. These structures might be used as potential flavonol analogs. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：7037 / 7039

页数：3

共 16 条

[11]

HARBORNE JB, 1994, FLAVONOIDS ADV RES S

[12] SYNTHESIS AND CYTOTOXICITY OF 1,6,7,8-SUBSTITUTED 2-(4'SUBSTITUTED PHENYL)-4-QUINOLONES AND RELATED-COMPOUNDS - IDENTIFICATION AS ANTIMITOTIC AGENTS INTERACTING WITH TUBULIN [J].