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Mendeleev Communications, 2016, Volume 26, Issue 5, Pages 375–377
DOI: https://doi.org/10.1016/j.mencom.2016.09.002
(Mi mendc2217)
 

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

Communications

Tandem AN–AN reactions in the synthesis of tetrahydrothiazolo[4,5-e][1,2,4]triazines

N. N. Mochulskayaab, P. A. Slepukhinab, V. N. Charushinab, M. I. Kodessab

a Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Full-text PDF (364 kB) Citations (3)
Abstract: Reaction of 3-aryl-1,2,4-triazines with S,N-dinucleophilic N-(het)arylthioureas in acetic anhydride at room temperature affords the cyclization products, tetrahydrothiazolo[4,5-e]-[1,2,4]triazines in good yields. The structure of the heterocyclic system thus formed was confirmed by X-ray diffraction analysis.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.2 Mb)


Citation: N. N. Mochulskaya, P. A. Slepukhin, V. N. Charushin, M. I. Kodess, “Tandem AN–AN reactions in the synthesis of tetrahydrothiazolo[4,5-e][1,2,4]triazines”, Mendeleev Commun., 26:5 (2016), 375–377
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  • https://www.mathnet.ru/eng/mendc2217
  • https://www.mathnet.ru/eng/mendc/v26/i5/p375
  • This publication is cited in the following 3 articles:
    1. S.M. Ivanov, Comprehensive Heterocyclic Chemistry IV, 2022, 29  crossref
    2. S. M. Ivanov, L. M. Mironovich, N. G. Kolotyrkina, A. M. Shestopalov, “Synthesis and chemical properties of 8-lithio-4-oxopyrazolo[5,1-c][1,2,4]triazines”, Russ Chem Bull, 68:3 (2019), 614  crossref
    3. S. M. Ivanov, L. M. Mironovich, L. A. Rodinovskaya, A. M. Shestopalov, “Synthesis of new 4-oxo-1,2,3,4-tetrahydropyrazolo[5,1-s][1,2,4]triazines”, Russ Chem Bull, 67:8 (2018), 1487  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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