4-(4-Methyl-1-piperazinyl)-7-trifluoromethylpyrrolo[1,2-a]quinoxaline (CGS 12066B) and related analogs were prepared in good overall yield through a reaction sequence involving as a key step the intramolecular substitution of aromatic fluoride or nitro groups by a carboxamide moiety. © 1991, Taylor & Francis Group, LLC. All rights reserved.
Campiani, G., Nacci, V., Corelli, F., Anzini, M. (1991). Polycondensed heterocycles. VII. A convenient synthesis of pyrrolo[1,2-a]quinoxaline derivatives by intramolecular aromatic nucleophilic displacement. SYNTHETIC COMMUNICATIONS, 21(15-16), 1567-1576 [10.1080/00397919108021054].
Polycondensed heterocycles. VII. A convenient synthesis of pyrrolo[1,2-a]quinoxaline derivatives by intramolecular aromatic nucleophilic displacement
Campiani G.;Nacci V.;Corelli F.;Anzini M.
1991-01-01
Abstract
4-(4-Methyl-1-piperazinyl)-7-trifluoromethylpyrrolo[1,2-a]quinoxaline (CGS 12066B) and related analogs were prepared in good overall yield through a reaction sequence involving as a key step the intramolecular substitution of aromatic fluoride or nitro groups by a carboxamide moiety. © 1991, Taylor & Francis Group, LLC. All rights reserved.
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https://hdl.handle.net/11365/29894
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