Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 1995, Volume 5, Issue 2, Pages 56–58
DOI: https://doi.org/10.1070/MC1995v005n02ABEH000455
(Mi mendc5029)
 

This article is cited in 24 scientific papers (total in 24 papers)

The Schmidt Rearrangement of Methyl Furoxanyl Ketones and Furoxancarboxylic Acids: a New Synthetic Route to Aminofuroxans

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

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The Schmidt rearrangement of methyl furoxanyl ketones and furoxancarboxylic acids has been carried out for the first time, exemplified by 3,4-diacetylfuroxan and 4-carboxy-3-(ethoxycarbonyl)furoxan, and this reaction has been shown to be a convenient method for the preparation of aminofuroxans.
Document Type: Article
Language: English


Citation: N. N. Makhova, A. N. Blinnikov, L. I. Khmel'nitskii, “The Schmidt Rearrangement of Methyl Furoxanyl Ketones and Furoxancarboxylic Acids: a New Synthetic Route to Aminofuroxans”, Mendeleev Commun., 5:2 (1995), 56–58
Linking options:
  • https://www.mathnet.ru/eng/mendc5029
  • https://www.mathnet.ru/eng/mendc/v5/i2/p56
  • This publication is cited in the following 24 articles:
    1. Muhammad Abu Yousef, Ryosuke Matsubara, “Recent progress in synthesis and application of furoxan”, RSC Adv., 13:8 (2023), 5228  crossref
    2. Lyudmila Larina, “The Structure of Biologically Active Functionalized Azoles: NMR Spectroscopy and Quantum Chemistry”, Magnetochemistry, 8:5 (2022), 52  crossref
    3. Qi Zhang, Cheng Zhao, Xun Zhang, Chunlin He, Siping Pang, “Oxidation of o-dioxime by (diacetoxyiodo)benzene: green and mild access to furoxans”, New J. Chem., 46:4 (2022), 1489  crossref
    4. Dmitry M. Bystrov, Leonid L. Fershtat, Nina N. Makhova, “Synthesis and reactivity of aminofuroxans”, Chem Heterocycl Comp, 55:12 (2019), 1143  crossref
    5. V. P. Zelenov, I. V. Fedyanin, D. V. Khakimov, T. S. Pivina, “Transformations of 3(4)-amino-4(3)-(tert-butyl-NNO-azoxy)furoxans in the annulation reactions into 1,2,3,4-tetrazine 1,3-dioxides”, Russ Chem Bull, 66:7 (2017), 1240  crossref
    6. Leonid L. Fershtat, Alexander S. Kulikov, Ivan V. Ananyev, Marina I. Struchkova, Nina N. Makhova, “New Method for the Synthesis and Reactivity of (5‐R‐1,3,4‐Oxadiazol‐2‐yl)furoxans”, Journal of Heterocyclic Chem, 53:1 (2016), 102  crossref
    7. 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
    8. Nina N. Makhova, Igor V. Ovchinnikov, Alexandr S. Kulikov, Dmitriy V. Khakimov, Marina S. Molchanova, Tatyana S. Pivina, “Diaminofuroxan: Synthetic Approaches and Computer‐Aided Study of Thermodynamic Stability”, Propellants Explo Pyrotec, 37:5 (2012), 549  crossref
    9. Aaron Wrobleski, Thomas C. Coombs, Chan Woo Huh, Sze‐Wan Li, Jeffrey Aubé, Organic Reactions, 2012, 1  crossref
    10. Comprehensive Organic Name Reactions and Reagents, 2010, 2503  crossref
    11. A. O. Finogenov, M. A. Epishina, A. S. Kulikov, N. N. Makhova, I. V. Anan'ev, V. A. Tartakovsky, “Synthesis and nitration of N,N´-bis(3-R-furoxan-4-yl)methylenediamines”, Russ Chem Bull, 59:11 (2010), 2108  crossref
    12. L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 157  crossref
    13. I. V. Ovchinnikov, A. O. Finogenov, M. A. Epishina, Yu. A. Strelenko, N. N. Makhova, “Synthesis of 1,3- and 1,4-bis(3-nitrofurazan-4-yl)benzenes and isomeric 1,3- and 1,4-bis[3(4)-nitrofuroxan-4(3)-yl]benzenes”, Mendeleev Commun., 19:4 (2009), 217–219  mathnet  crossref
    14. I. V. Ovchinnikov, K. A. Lyssenko, N. N. Makhova, “An unexpected transformation of 3,4-bis(isocyanato)furoxan into 3,3'-bi(1,2,4-oxadiazol-5-one)”, Mendeleev Commun., 19:3 (2009), 144–146  mathnet  crossref
    15. S. I. Molotov, M. A. Epishina, A. S. Kulikov, Yu. V. Nelyubina, K. A. Lyssenko, K. Yu. Suponitsky, N. N. Makhova, “Thermally induced rearrangement of the arylhydrazones of furoxan-3-yl carbonyl compounds”, Mendeleev Commun., 16:5 (2006), 259–262  mathnet  crossref
    16. 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
    17. S. I. Molotov, A. S. Kulikov, N. N. Makhova, K. A. Lyssenko, “Thermal rearrangements of 3-substituted 4-(3-ethoxycarbonylthioureido)-1,2,5-oxadiazole 2-oxides”, Mendeleev Commun., 13:4 (2003), 188–190  mathnet  crossref
    18. Olga V. Donskaya, Valentina N. Elokhina, Anatoly S. Nakhmanovich, Tamara I. Vakul'skaya, Lyudmila I. Larina, Aleksandr I. Vokin, Aleksandr I. Albanov, Valentin A. Lopyrev, “Vicarious C-amination of 1-methyl-4-nitroimidazole”, Tetrahedron Letters, 43:37 (2002), 6613  crossref
    19. Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65  crossref
    20. A. N. Blinnikov, N. N. Makhova, L. I. Khmel'nitskii, “New approaches to the preparation of azoxyfuroxans”, Mendeleev Commun., 9:1 (1999), 15–17  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:26
    Full-text PDF :5
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025