Polycondensed heterocycles. VII. A convenient synthesis of pyrrolo[1,2-a]quinoxaline derivatives by intramolecular aromatic nucleophilic displacement

Article abstract of DOI:10.1080/00397919108021054

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 in the intramolecular substitution of aromatic fluoride or nitr

Full text of DOI:10.1080/00397919108021054

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Polycondensed Heterocycles.
VII. A Convenient Synthesis
of Pyrrolo[1,2-a]quinoxaline
Derivatives by Intramolecular
Aromatic Nucleophilic
Displacement
G. Campiani a , V. Nacci a , F. Corelli a & M. Anzini a
a Dipartimento Farmaco Chimico Tecnologico ,
Università di Siena , Banchi di Sotto 55, 53100,
Siena, Italy
Published online: 23 Sep 2006.
To cite this article: G. Campiani , V. Nacci , F. Corelli & M. Anzini (1991)
Polycondensed Heterocycles. VII. A Convenient Synthesis of Pyrrolo[1,2-a]quinoxaline
Derivatives by Intramolecular Aromatic Nucleophilic Displacement, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:15-16, 1567-1576, DOI: 10.1080/00397919108021054
To link to this article: http://dx.doi.org/10.1080/00397919108021054
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