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
收藏
页码：3047 / 3050
页数：4
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