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Mendeleev Communications, 1994, Volume 4, Issue 3, Pages 104–107
DOI: https://doi.org/10.1070/MC1994v004n03ABEH000371
(Mi mendc5175)
 

This article is cited in 7 scientific papers (total in 7 papers)

Reactions of Diazido Derivatives of s-Triazine with C-Nucleophiles

Yu. A. Azeva, I. P. Loginovab, O. L. Guselnikovab, S. V. Shorshneva, V. L. Rusinovc, O. N. Chupakhind

a Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
b Urals Polytechnical Institute, Ekaterinburg, Russian Federation
c Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
d I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Full-text PDF (277 kB) Citations (7)
Abstract: The reaction of 2,4-diazido-s-triazines 1 with an equimolar amount or a two-fold molar excess of ethyl cyanoacetate in the presence of triethylamine in DMF affords the corresponding mono- 2 or diamino derivatives of s-triazine 3; on heating 2,4-diazido-s-triazines 1ad with a two-fold molar excess of acetoacetone or ethyl acetoacetate in the presence of triethylamine in ethanol the corresponding 1,2,3-triazolo-s-triazines 4af are formed.
Document Type: Article
Language: English


Citation: Yu. A. Azev, I. P. Loginova, O. L. Guselnikova, S. V. Shorshnev, V. L. Rusinov, O. N. Chupakhin, “Reactions of Diazido Derivatives of s-Triazine with C-Nucleophiles”, Mendeleev Commun., 4:3 (1994), 104–107
Linking options:
  • https://www.mathnet.ru/eng/mendc5175
  • https://www.mathnet.ru/eng/mendc/v4/i3/p104
  • This publication is cited in the following 7 articles:
    1. L. V. Batog, V. Yu. Rozhkov, M. I. Struchkova, A. S. Kulikov, N. N. Makhova, “Synthesis of N,N′-bis[4-(1H-1,2,3-triazol-1-yl)furazan-3-yl]-methylenediamine derivatives”, Russ Chem Bull, 62:6 (2013), 1391  crossref
    2. Svetlana Mikhaylichenko, Anthony Veloso, Kunjal Patel, Vladimir Zaplishny, “Synthesis and structure of new 1,2,3-triazolyl substituted 1,3,5-triazines”, Eur. J. Chem., 3:1 (2012), 1  crossref
    3. V. Yu. Rozhkov, L. V. Batog, M. I. Struchkova, “Synthesis of 1,2,4-oxadiazole-, pyrrole- and 1,2,3-triazole-substituted (1,2,3-triazol-1-yl)furazans”, Mendeleev Commun., 18:3 (2008), 161–163  mathnet  crossref
    4. L. V. Batog, V. Yu. Rozhkov, M. I. Struchkova, “Azido-1,2,5-oxadiazoles in reactions with 1,3-dicarbonyl compounds”, Mendeleev Commun., 12:4 (2002), 159–162  mathnet  crossref
    5. E. B. Nikolaenkova, V. P. Krivopalov, “Synthesis of 4,6-bis(1H-1,2,3-triazolyl)pyrimidines by the reaction of 4,6-diazido-2-(4-methoxyphenyl)-pyrimidine with compounds containing a reactive methylene group”, Chem Heterocycl Compd, 33:8 (1997), 968  crossref
    6. Derek T. Hurst, Progress in Heterocyclic Chemistry, 7, 1995, 244  crossref
    7. YU. A. AZEV, I. P. LOGINOVA, O. L. GUSELNIKOVA, S. V. SHORSHNEV, V. L. RUSINOV, O. N. CHUPAKHIN, “ChemInform Abstract: Reactions of Diazido Derivatives of s‐Triazine with C‐Nucleophiles.”, ChemInform, 25:43 (1994)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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