Abstract
The synthesis of bis(indol-1-yl)maleimides and polycondenced diazepines[1,4], which contain various functional groups and are the analogs of biologically active indolo[2,3-а]carbazoles, is described. Functional groups were introduced directly into diazepine and bis-indolylmaleimide molecules via eletrophilic substitution reactions using precursors containing such functional groups.
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