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Mendeleev Communications, 1999, Volume 9, Issue 5, Pages 200–201
DOI: https://doi.org/10.1070/MC1999v009n05ABEH001169
(Mi mendc4596)
 

This article is cited in 3 scientific papers (total in 3 papers)

Regiospecific cleavage of a triazole or pyrimidine ring in nitrotriazolo[1,5-a]pyrimidones

V. V. Voronina, E. N. Ulomskya, V. L. Rusinova, O. N. Chupakhinb

a Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
b I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Full-text PDF (149 kB) Citations (3)
Abstract: The reaction of nitrotriazolo[1,5-a]pyrimidines 1 with primary amines leads to cleavage of the pyrimidine ring, whereas triazole ring opening takes place in the reaction of 1 with secondary amines.
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Document Type: Article
Language: English


Citation: V. V. Voronin, E. N. Ulomsky, V. L. Rusinov, O. N. Chupakhin, “Regiospecific cleavage of a triazole or pyrimidine ring in nitrotriazolo[1,5-a]pyrimidones”, Mendeleev Commun., 9:5 (1999), 200–201
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  • https://www.mathnet.ru/eng/mendc/v9/i5/p200
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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