Cyclization of N-alkylazinium cations with bifunctional nucleophiles. 14. Reaction of quinoxalinium salts with mono- and N,N′-disubstituted amidines |
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Authors: | L. M. Naumova V. N. Charushin O. N. Chupakhin G. G. Izmailova |
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Affiliation: | (1) S. M. Kirov Ural Polytechnic Institute, 620002 Sverdlovsk |
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Abstract: | Monosubstituted benzamidines undergo cyclization with quinoxalinum salts to give 1,2-disubstituted 3a,4,9,9a-tetrahydroimidazo[4,5-b]quinoxalines. The participation in similar cyclizations of N,N-disubstituted amidines with a CH-active group in the a position leads to 3a,4,9,9a-tetrahydropyrrolo[2,3-b]quinoxalines.See [1] for Communication 13.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 390–395, March, 1985. |
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