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Mendeleev Communications, 1997, Volume 7, Issue 4, Pages 164–165
DOI: https://doi.org/10.1070/MC1997v007n04ABEH000793
(Mi mendc4837)
 

This article is cited in 4 scientific papers (total in 4 papers)

Transformations of 5-azauracil in reactions with some nucleophiles

Yu. A. Azev

Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
Full-text PDF (69 kB) Citations (4)
Abstract: Heating 5-azauracil 1 with 3-methyl-1-phenylpyrazol-5-one 2 in boiling butanol gave dipyrazolylmethane 3 and biuret 4; under similar conditions, indoles 5 react with 1 to yield stable 6-indolyl derivatives of 2,4-dioxohexahydro-s-triazine 6.1Fax: +7 3432 22 0781.
Document Type: Article
Language: English


Citation: Yu. A. Azev, “Transformations of 5-azauracil in reactions with some nucleophiles”, Mendeleev Commun., 7:4 (1997), 164–165
Linking options:
  • https://www.mathnet.ru/eng/mendc4837
  • https://www.mathnet.ru/eng/mendc/v7/i4/p164
  • This publication is cited in the following 4 articles:
    1. O. N. Chupakhin, I. N. Egorov, V. L. Rusinov, P. A. Slepukhin, “Asymmetric induction in the reactions of azinones with C-nucleophiles”, Russ Chem Bull, 59:5 (2010), 991  crossref
    2. Yu. A. Azev, S. V. Shorshnev, D. Gabel, “Stable σ-adducts of 5-azauracil with C-nucleophiles”, Mendeleev Commun., 11:6 (2001), 234–235  mathnet  crossref
    3. Yu. A. Azev, I. V. Teplyashina, “Reaction of dipyrazolylmethanes with 1-phenyl-3-methylpyrazol-5-one”, Chem Heterocycl Compd, 34:9 (1998), 1091  crossref
    4. YU. A. AZEV, “ChemInform Abstract: Transformations of 5‐Azauracil in Reactions with Some Nucleophiles.”, ChemInform, 28:47 (1997)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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