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Mendeleev Communications, 1996, Volume 6, Issue 1, Pages 11–12
DOI: https://doi.org/10.1070/MC1996v006n01ABEH000555
(Mi mendc4889)
 

This article is cited in 13 scientific papers (total in 13 papers)

N-Nitropyrazoles, a new source of nitrogen monoxide

N. B. Grigorieva, V. I. Levinaa, S. A. Shevelevb, I. L. Dalingerb, V. G. Granikc

a Centre for Medicinal Chemistry. Sergo Ordzhonikidze All-Russian Research Chemical-Pharmaceutical Institute, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Russian Research Centre 'Research Institute of Organic Intermediates and Dyes', Moscow, Russian Federation
Abstract: Electrochemical reduction of N-nitropyrazoles, and chemical reduction by cysteine or potassium ferrocyanide, results in nitrogen monoxide.
Document Type: Article
Language: English


Citation: N. B. Grigoriev, V. I. Levina, S. A. Shevelev, I. L. Dalinger, V. G. Granik, “N-Nitropyrazoles, a new source of nitrogen monoxide”, Mendeleev Commun., 6:1 (1996), 11–12
Linking options:
  • https://www.mathnet.ru/eng/mendc4889
  • https://www.mathnet.ru/eng/mendc/v6/i1/p11
  • This publication is cited in the following 13 articles:
    1. Tatyana K. Shkineva, Svetlana A. Krasnova, Igor L. Dalinger, “The first example of a cine-substitution in a series of 1,3-dinitropyrazoles”, Chem Heterocycl Comp, 60:5-6 (2024), 257  crossref
    2. Alexandr V. Kormanov, Dmitry L. Lipilin, Tatyana K. Shkineva, Irina A. Vatsadze, Andrei M. Kozeev, Igor L. Dalinger, “Synthesis and transformations of 3(5)-(3-methylfurazan-4-yl)-4-nitro-1N-pyrazole-5(3)-carboxylic acid”, Chem Heterocycl Comp, 53:8 (2017), 876  crossref
    3. Irina A. Vatsadze, Olga V. Serushkina, Mikhail D. Dutov, Tatyana K. Shkineva, Kyrill Yu. Suponitsky, Bogdan I. Ugrak, Igor L. Dalinger, “Synthesis of 1-(N-nitropyrazolyl)-1N-tetrazoles – a new type of heteronuclear N-nitropyrazole derivatives”, Chem Heterocycl Comp, 51:8 (2015), 695  crossref
    4. L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 407  crossref
    5. L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 1  crossref
    6. L. Yet, Comprehensive Heterocyclic Chemistry III, 2008, 1  crossref
    7. L. A. Trukhacheva, V. I. Levina, N. B. Grigor'ev, A. P. Arzamastsev, I. L. Dalinger, I. A. Vatsadze, G. P. Popova, S. A. Shevelev, V. G. Granik, “Kinetics of hydrolysis of five-membered C-nitroheterocycles: pyrazole, imidazole, 1,2,4-triazole, and isoxazole derivatives”, Russ Chem Bull, 54:12 (2005), 2813  crossref
    8. V. I. Levina, A. V. Danilov, N. B. Grigor'ev, “Polarographic detection of nitric oxide during the oxidation of some nitrogen-containing organic compounds by potassium ferricyanide”, Pharm Chem J, 32:4 (1998), 226  crossref
    9. N. B. Grigor'ev, M. I. Kalinkina, G. V. Chechekin, V. B. Nikitin, G. N. Engalycheva, N. N. Belushkina, V. I. Levina, I. L. Dalinger, M. D. Mashkovskii, S. A. Shevelev, V. A. Litosh, M. V. Vener, I. S. Severina, M. É. Kaminka, A. P. Arzamastsev, V. G. Granik, “N-nitropyrazoles: A new class of nitrogen oxide generators”, Pharm Chem J, 32:3 (1998), 127  crossref
    10. I. L. Dalinger, V. A. Litosh, S. A. Shevelev, “Nitropyrazoles”, Russ Chem Bull, 46:6 (1997), 1149  crossref
    11. L. N. Koikov, N. V. Alekseeva, N. B. Grigor'ev, V. I. Levina, K. F. Turchin, T. Ya. Filipenko, M. D. Mashkovskii, M. É. Kaminka, V. B. Nikitin, G. N. Engalycheva, M. I. Kalinkina, V. G. Granik, I. S. Severina, I. K. Ryaposova, “Search for no donors. Part I. 3-Quinuclidone oximes”, Pharm Chem J, 31:5 (1997), 243  crossref
    12. N. B. GRIGOR'EV, V. I. LEVINA, S. A. SHEVELEV, I. L. DALINGER, V. G. GRANIK, “ChemInform Abstract: N‐Nitropyrazoles, a New Source of Nitrogen Monoxide.”, ChemInform, 27:25 (1996)  crossref
    13. L. N. Koikov, N. V. Alekseeva, N. B. Grigoriev, V. I. Levina, K. F. Turchin, T. Ya. Filipenko, I. S. Severina, I. K. Ryaposova, V. G. Granik, “Oximes of quinuclidin-3-ones as nitric oxide donors”, Mendeleev Commun., 6:3 (1996), 94–96  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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