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Mendeleev Communications, 1996, Volume 6, Issue 5, Pages 190–191
DOI: https://doi.org/10.1070/MC1996v006n05ABEH000639
(Mi mendc4973)
 

This article is cited in 9 scientific papers (total in 9 papers)

A route to pyrazolylazopyrazolo[4,3-c]pyrazoles via l,5-dimethyl-3R-pyrazolyl-4-diazonium salts

E. V. Tretyakov, S. F. Vasilevskii

V.V. Voevodsky Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Full-text PDF (253 kB) Citations (9)
Abstract: l,5-Dimethyl-3R-pyrazolyl-4-diazonium salts (R = H, C ≡ C–Ph) have been converted into the corresponding 6-(l,5-dimethyl-3R-pyrazol-4-yl)azo-l-methyl-3R-4H-pyrazolo[4,3-c]pyrazoles 6a,b and it has been shown that the reaction proceeds via l-methyl-5-(l,5-dimethyl-3R-pyrazolyl-4-azo)methyl-3R-pyrazolyl-4-diazonium chlorides 4a,b.
Document Type: Article
Language: English


Citation: E. V. Tretyakov, S. F. Vasilevskii, “A route to pyrazolylazopyrazolo[4,3-c]pyrazoles via l,5-dimethyl-3R-pyrazolyl-4-diazonium salts”, Mendeleev Commun., 6:5 (1996), 190–191
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  • https://www.mathnet.ru/eng/mendc/v6/i5/p190
  • This publication is cited in the following 9 articles:
    1. Adam Campbell, Paul W. Peterson, Igor V. Alabugin, Aromaticity, 2021, 339  crossref
    2. Paul W. Peterson, Rana K. Mohamed, Igor V. Alabugin, “How to Lose a Bond in Two Ways ― The Diradical/Zwitterion Dichotomy in Cycloaromatization Reactions”, Eur J Org Chem, 2013:13 (2013), 2505  crossref
    3. Rana K. Mohamed, Paul W. Peterson, Igor V. Alabugin, “Concerted Reactions That Produce Diradicals and Zwitterions: Electronic, Steric, Conformational, and Kinetic Control of Cycloaromatization Processes”, Chem. Rev., 113:9 (2013), 7089  crossref
    4. Shivaji S. Kadam, Lukáš Maier, Ioannis Kostakis, Nicole Pouli, Jaromír Toušek, Marek Nečas, Panagiotis Marakos, Radek Marek, “Synthesis and Tautomerism of Substituted Pyrazolo[4,3‐c]pyrazoles”, Eur J Org Chem, 2013:30 (2013), 6811  crossref
    5. Pablo López-Tarifa, Goar Sánchez-Sanz, Ibon Alkorta, José Elguero, Dionisia Sanz, Almudena Perona, Rosa M. Claramunt, “The tautomeric structures of 3(5),3′(5′)-azopyrazole [(E)-1,2-di(1H-pyrazol-3(5)-yl)diazene)]: The combined use of NMR and electronic spectroscopies with DFT calculations”, Journal of Molecular Structure, 1015 (2012), 138  crossref
    6. Sergei F Vasilevsky, Eugene V Tretyakov, José Elguero, Advances in Heterocyclic Chemistry, 82, 2002, 1  crossref
    7. Eugene V. Tretyakov, Sergei F. Vasilevsky, “NEW FINDINGS IN THE RICHTER REACTION IN SERIES OF VICINAL ALKYNYLPYRAZOLYLDIAZONIUM SALTS”, Heterocyclic Communications, 4:6 (1998)  crossref
    8. E. V. TRETYAKOV, S. F. VASILEVSKY, “ChemInform Abstract: A Route to Pyrazolylazopyrazolo(4,3‐c)pyrazoles (III) via 1,5‐Dimethyl‐ 3R‐pyrazolyl‐4‐diazonium Salts (II).”, ChemInform, 28:9 (1997)  crossref
    9. E. V. Tret'yakov, S. F. Vasitevsky, “Synthesis of vicinal aminoiodo- and (acetylamino)iodo-l-alkylpyrazoles”, Russ Chem Bull, 45:11 (1996), 2585  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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