Diazepines[1,4] annelated with indoline and maleimide from 3-(di)alkylamino-4-(indol-1-yl)maleimides: mechanism of rearrangement and cyclization

被引:7
作者
Lakatosh, SA [1 ]
Luzikov, YN [1 ]
Preobrazhenskaya, MN [1 ]
机构
[1] Russian Acad Med Sci, Gause Inst New Antibiot, Moscow 119021, Russia
基金
俄罗斯基础研究基金会;
关键词
cyclization; hydride shift; mechanism; indole;
D O I
10.1016/j.tet.2005.01.005
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The mechanism of cyclization of 3-(di)alkylamino-4-(indol-1-yl)maleimides to diazepine[1,4] derivatives was elucidated using deuterium labeled precursors. (C) 2005 Published by Elsevier Ltd.
引用
收藏
页码:2017 / 2020
页数:4
相关论文
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[1]   Synthesis of 6H-pyrrolo[3′,4′:2,3][1,4]diazepino[6,7,1-hi]indole-8,10(7H,9H)-diones using 3-bromo-4-(indol-1-yl)maleimide scaffold [J].
Lakatosh, SA ;
Luzikov, YN ;
Preobrazhenskaya, MN .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (05) :826-833