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Synthesis of 1,2,3-triazolo[1,5-а]pyridin-8-ium-3-olates

Инна С. Хажиева, Павел М. Дёмкин, Юлия И. Нейн, Татьяна В. Глухарева, Юрий Ю. Моржерин
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Alkylation of sodium 4-acetyl-1-phenyl-1,2,3-triazol-5-olate with α-bromoacetophenones was shown to occur at position 3 of the heterocycle, with the formation of 1,2,3-triazol-3-ium-5-olates. Intramolecular crotonic condensation of the latter led to the formation of 1,2,3-triazolo[1,5-а]pyridin-8-ium-3-olates.

How to Cite
Khazhieva, I. S.; Demkin, P. M.; Nein, Y. I.; Glukhareva, T. V.; Morzherin, Y. Yu. Chem. Heterocycl. Compd. 2015, 51, 199. [Khim. Geterotsikl. Soedin. 2015, 51, 199.]

For this article in the English edition see DOI 10.1007/s10593-015-1681-x



azoles; fused heterocycles; mesoionic heterocycles; pyridines; 1,2,3-triazoles; 1,2,3-triazol-3-ium-5-olates; alkylation; crotonic condensation; heterocyclization

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