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Mendeleev Communications, 1999, Volume 9, Issue 1, Pages 15–17
DOI: https://doi.org/10.1070/MC1999v009n01ABEH000994
(Mi mendc4506)
 

This article is cited in 15 scientific papers (total in 15 papers)

New approaches to the preparation of azoxyfuroxans

A. N. Blinnikov, N. N. Makhova, L. I. Khmel'nitskii

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (78 kB) Citations (15)
Abstract: A new convenient method for the synthesis of 4,4′-azoxyfuroxans by reductive condensation of 4-nitrofuroxans (4-nitro-1,2,5-oxadiazole 2-oxides) has been developed; the title compounds can also be synthesised by oxidation of 4-amino- and 4,4′-azofuroxans, and a general method for the synthesis of isomeric azofuroxans is suggested.
Document Type: Article
Language: English


Citation: A. N. Blinnikov, N. N. Makhova, L. I. Khmel'nitskii, “New approaches to the preparation of azoxyfuroxans”, Mendeleev Commun., 9:1 (1999), 15–17
Linking options:
  • https://www.mathnet.ru/eng/mendc4506
  • https://www.mathnet.ru/eng/mendc/v9/i1/p15
  • This publication is cited in the following 15 articles:
    1. Dmitry M. Bystrov, Leonid L. Fershtat, Nina N. Makhova, “Synthesis and reactivity of aminofuroxans”, Chem Heterocycl Comp, 55:12 (2019), 1143  crossref
    2. V. V. Parakhin, P. B. Gordeev, O. A. Luk'yanov, “3-(1-Methyl-1-nitroethyl-1-ONN-azoxy)-4-aminofuroxan. Synthesis and transformations of the amino group”, Russ Chem Bull, 67:6 (2018), 1065  crossref
    3. B. V. Lyalin, V. L. Sigacheva, L. L. Fershtat, N. N. Makhova, V. A. Petrosyan, “Eco-friendly N–N coupling of aminofuroxans into azofuroxans under the action of electrogenerated hypohalites”, Mendeleev Commun., 28:5 (2018), 518–520  mathnet  crossref
    4. Qi Wang, Tian Lu, Chenbin Wang, Guijuan Fan, Hongquan Yin, Fu-Xue Chen, “Synthesis of 5,5′-azoxybistetrazole via nitration and de-oxygen rearrangement of triazene”, New J. Chem., 41:20 (2017), 11512  crossref
    5. N. N. Makhova, A. S. Kulikov, “Advances in the chemistry of monocyclic amino- and nitrofuroxans”, Russian Chem. Reviews, 82:11 (2013), 1007–1033  mathnet  mathnet  crossref  isi  scopus
    6. L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 1  crossref
    7. G. Nikonov, S. Bobrov, Comprehensive Heterocyclic Chemistry III, 2008, 315  crossref
    8. I.V Ovchinnikov, A.S Kulikov, N.N Makhova, P Tosco, A Di Stilo, R Fruttero, A Gasco, “Synthesis and vasodilating properties of N-alkylamide derivatives of 4-amino-3-furoxancarboxylic acid and related azo derivatives”, Il Farmaco, 58:9 (2003), 677  crossref
    9. I. V. Ovchinnikov, M. A. Epishina, S. I. Molotov, Yu. A. Strelenko, K. A. Lyssenko, N. N. Makhova, “New rearrangement of azofuroxans in an oxidising medium”, Mendeleev Commun., 13:6 (2003), 272–275  mathnet  crossref
    10. D. Yu. Tsvetkov, S. I. Blinnikov, N. N. Pavlyuk, “Radial distributions of gamma-ray bursts and type Ib/c supernovae in galaxies”, Astron. Lett., 27:7 (2001), 411  crossref
    11. Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65  crossref
    12. Andreu Balastegui, Pilar Ruiz-Lapuente, Ramon Canal, “Reclassification of gamma-ray bursts”, Monthly Notices of the Royal Astronomical Society, 328:1 (2001), 283  crossref
    13. S. S. Gershtein, “Oscillation structure of gamma-ray bursts and their possible origin”, Astron. Lett., 26:11 (2000), 730  crossref
    14. Alexander N. Blinnikov, Nina N. Makhova, Lenor I. Khmel'nitskii, “ChemInform Abstract: New Approaches to the Preparation of Azoxyfuroxans.”, ChemInform, 30:29 (1999)  crossref
    15. N. N. Makhova, A. N. Blinnikov, “New version of mononuclear heterocyclic rearrangement”, Mendeleev Commun., 9:1 (1999), 17–19  mathnet  crossref
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