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A single step synthesis of 6-aminophenanthridines from anilines and 2-chlorobenzonitriles
Authors:Fabienne Gug  Marc Blondel  Anne-Sophie Martin
Affiliation:a Laboratoire de Chimie Organique, Université René Descartes, 4 avenue de l'Observatoire, 75006 Paris, France
b C.N.R.S., Station Biologique, Cell Cycle Laboratory, place G. Teissier, 29680 Roscoff, Bretagne, France
Abstract:
Biologically active 6-aminophenanthridines were prepared in a single step procedure: Metal amides in liquid ammonia promoted the condensation of anilines with 2-chloro-benzonitriles. 6-Aminophenanthridines were isolated in moderate yield.
Keywords:Amidine   Prions   Phenanthridine   Heterocyclisation
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