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Mendeleev Communications, 2004, Volume 14, Issue 2, Pages 76–77
DOI: https://doi.org/10.1070/MC2004v014n02ABEH001891
(Mi mendc3814)
 

This article is cited in 23 scientific papers (total in 23 papers)

Synthesis and Dimroth rearrangement of 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles

V. Yu. Rozhkov, L. V. Batog, E. K. Shevtsova, M. I. Struchkova

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (88 kB) Citations (23)
Abstract: The cycloaddition of 4-amino-3-azido-1,2,5-oxadiazole to nitriles with activated methylene groups has been studied, and 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles and the products of their Dimroth rearrangement, viz, N-(4-R-1H-1,2,3-triazol-5-yl)-1,2,5-oxadiazole-3,4-diamines, have been synthesised.
Document Type: Article
Language: English


Citation: V. Yu. Rozhkov, L. V. Batog, E. K. Shevtsova, M. I. Struchkova, “Synthesis and Dimroth rearrangement of 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles”, Mendeleev Commun., 14:2 (2004), 76–77
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  • https://www.mathnet.ru/eng/mendc/v14/i2/p76
  • This publication is cited in the following 23 articles:
    1. Sofya P. Balabanova, Alexey A. Voronin, Aleksandr M. Churakov, Michael S. Klenov, Vladimir A. Tartakovsky, “Synthetic Strategies for C‐Amino 1,2,3‐Triazoles and Their Oxides: A Review”, Journal of Heterocyclic Chem, 61:12 (2024), 2106  crossref
    2. G. V. Tsaplin, S. V. Popkov, “Intramolecular ANRORC Reactions in the Series of Diazoles with Three Heteroatoms”, Russ J Org Chem, 58:1 (2022), 1  crossref
    3. Ziqi Su, Hongxin Chai, Juan Xu, Jiarong Li, “ZnCl2-promoted domino reaction of 2-hydroxybenzonitriles with ketones for synthesis of 1,3-benzoxazin-4-ones”, RSC Adv., 11:48 (2021), 29906  crossref
    4. Vitor F. Ferreira, Thais de B. da Silva, Fernanda P. Pauli, Patricia G. Ferreira, Luana da S. M. Forezi, Carolina G. de S. Lima, Fernando de C. da Silva, “Dimroth´s Rearrangement as a Synthetic Strategy Towards New Heterocyclic Compounds”, COC, 24:17 (2020), 1999  crossref
    5. Moulay H. Youssoufi, Pramod K. Sahu, Praveen K. Sahu, Dau D. Agarwal, Mushtaq Ahmad, Mouslim Messali, Siham Lahsasni, Taibi Ben Hadda, “POM analyses of antimicrobial activity of 4H-pyrimido[2,1-b]benzothiazole, pyrazole, and benzylidene derivatives of curcumin”, Med Chem Res, 24:6 (2015), 2381  crossref
    6. L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259  mathnet  crossref
    7. Chengming Bian, Kai Wang, Lixuan Liang, Man Zhang, Chuan Li, Zhiming Zhou, “Nitrogen‐Rich Energetic Salts of Bis‐Heterocycle‐Substituted 1,2,3‐Triazole (HTANFT)”, Eur J Inorg Chem, 2014:35 (2014), 6022  crossref
    8. L. V. Batog, V. Yu. Rozhkov, M. I. Struchkova, A. S. Kulikov, N. N. Makhova, “Synthesis of N,N′-bis[4-(1H-1,2,3-triazol-1-yl)furazan-3-yl]-methylenediamine derivatives”, Russ Chem Bull, 62:6 (2013), 1391  crossref
    9. L. V. Batog, L. S. Konstantinova, A. S. Kulikov, N. N. Makhova, “Synthesis of 4,4′-bis(dichloroamino)- and 4,4′-bis(chloroamino)-3,3′-azofurazans, the first representatives of dichloroamino- and chloroaminofurazans”, Russ Chem Bull, 62:6 (2013), 1388  crossref
    10. A. S. Kulikov, M. A. Epishina, L. V. Batog, V. Yu. Rozhkov, N. N. Makhova, L. D. Konyushkin, M. N. Semenova, V. V. Semenov, “Synthesis and antineoplastic properties of (1H-1,2,3-triazol-1-yl)furazans”, Russ Chem Bull, 62:3 (2013), 836  crossref
    11. Liupan Yang, Jiarong Li, Hongxin Chai, Hongyan Lu, Qi Zhang, Daxin Shi, “A Divergent Synthesis of 1,8‐Naphthyridines and Hydropyridopyrimidinones by the Reactions of o‐Aminonitriles with Ketones”, Chin. J. Chem., 31:4 (2013), 443  crossref
    12. Liupan Yang, Daxin Shi, Shu Chen, Hongxin Chai, Danfei Huang, Qi Zhang, Jiarong Li, “Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium”, Green Chem., 14:4 (2012), 945  crossref
    13. Name Reactions in Heterocyclic Chemistry II, 2011, 515  crossref
    14. V. Yu. Rozhkov, L. V. Batog, M. I. Struchkova, “Synthesis of 3-nitramino-4-(1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles and their salts”, Russ Chem Bull, 60:8 (2011), 1712  crossref
    15. Catherine J. Smith, Nikzad Nikbin, Steven V. Ley, Heiko Lange, Ian R. Baxendale, “A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles”, Org. Biomol. Chem., 9:6 (2011), 1938  crossref
    16. El Sayed H. El Ashry, Said Nadeem, Muhammad Raza Shah, Yeldez El Kilany, Advances in Heterocyclic Chemistry, 101, Advances in Heterocyclic Chemistry Volume 101, 2010, 161  crossref
    17. Comprehensive Organic Name Reactions and Reagents, 2010, 905  crossref
    18. Jian-Hong Tang, Da-Xin Shi, Li-Jun Zhang, Qi Zhang, Jia-Rong Li, “Facile and One-Pot Synthesis of 1,2-Dihydroquinazolin-4(3H)-ones via Tandem Intramolecular Pinner/Dimroth Rearrangement”, Synthetic Communications, 40:5 (2010), 632  crossref
    19. Li-Jun Zhang, Da-Xin Shi, Jia-Rong Li, “Simultaneous Synthesis of Pyrazolopyridines and Pyrazolopyrimidinones Under Microwave Irradiation”, Synthetic Communications, 39:22 (2009), 4010  crossref
    20. G. Nikonov, S. Bobrov, Comprehensive Heterocyclic Chemistry III, 2008, 315  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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