Original and rapid access to new alkaloid analogues of neocryptolepine:: Synthesis of substituted 6-methyl-6H-indolo[2,3-b]quinolines via TDAE strategy

被引：29

作者：

Amiri-Attou, O ^{[1
]}

Terme, T ^{[1
]}

Vanelle, P ^{[1
]}

机构：

[1] Univ Mediterranee, CNRS, UMR 6517, LCOP, F-13385 Marseille 05, France

来源：

SYNLETT | 2005年 / 20期

关键词：

TDAE; indolo[2,3-b]quinoline; alkaloids; reduction; 1-methyl isatin;

D O I：

10.1055/s-2005-921916

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We report herein an original and rapid synthesis of new substituted 6H-indolo[2,3-b]quinolines based on TDAE strategy from reaction between substituted o-nitrobenzyl chlorides and 1-methyl isatin followed by a one-pot reduction-cyclization-dehydration reaction.

引用

页码：3047 / 3050

页数：4