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dc.contributor.authorKorotina, A. V.en
dc.contributor.authorTolshchina, S. G.en
dc.contributor.authorIshmetova, R. I.en
dc.contributor.authorEvstigneeva, N. P.en
dc.contributor.authorGerasimova, N. A.en
dc.contributor.authorZilberberg, N. V.en
dc.contributor.authorKungurov, N. V.en
dc.contributor.authorRusinov, G. L.en
dc.contributor.authorChupakhin, O. N.en
dc.contributor.authorCharushin, V. N.en
dc.date.accessioned2022-10-19T05:22:38Z-
dc.date.available2022-10-19T05:22:38Z-
dc.date.issued2022-
dc.identifier.citationSynthesis of novel [1,2,4]triazolo[1,5-b][1,2,4,5]tetrazines and investigation of their fungistatic activity / A. V. Korotina, S. G. Tolshchina, R. I. Ishmetova et al. // Beilstein Journal of Organic Chemistry. — 2022. — Vol. 18. — P. 243-250.en
dc.identifier.issn18605397-
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85128396407&doi=10.3762%2fbjoc.18.29&partnerID=40&md5=66f471deb9801f1555b6d5758f5b4628link
dc.identifier.urihttp://elar.urfu.ru/handle/10995/118131-
dc.description.abstractA series of novel [1,2,4]triazolo[1,5-b][1,2,4,5]tetrazines has been synthesized through oxidation reaction of the corresponding 3,6-disubstituted 1,2,4,5-tetrazines bearing amidine fragments. It is shown that the heterocyclic systems obtained can be modified easily at C(3) position in the reactions with aliphatic alcohols and amines. Also, the reactivity of [1,2,4]triazolo[1,5-b][1,2,4,5]tetrazines towards CH-active compounds has been studied. The obtained triazolo[1,5-b]annulated 1,2,4,5-tetrazines proved to be active in micromolar concentrations in vitro against filamentous anthropophilic and zooanthropophilic dermatophyte fungi (Trichophyton, Microsporum and Epidermofiton), which cause skin and its appendages (hair, nails) diseases. © 2022 Korotina et al.; licensee Beilstein-Institut.en
dc.description.sponsorshipMinistry of Education and Science of the Russian Federation, Minobrnauka: 075-15-2020-777; Ural Branch, Russian Academy of Sciences, UB RASen
dc.description.sponsorshipThis work was supported by the Ministry of Education and Science of the Russian Federation (Agreement No. 075-15-2020-777).en
dc.description.sponsorshipAnalytical studies were carried out using equipment of the Center for Joint Use “Spectroscopy and Analysis of Organic Compounds”, located in Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences. This work was supported by the Ministry of Education and Science of the Russian Federation (Agreement No. 075-15-2020-777).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherBeilstein-Institut Zur Forderung der Chemischen Wissenschaftenen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceBeilstein Journal of Organic Chemistryen
dc.subjectANTIFUNGAL ACTIVITYen
dc.subjectNUCLEOPHILIC SUBSTITUTIONen
dc.subjectOXIDATIVE CYCLIZATIONen
dc.titleSynthesis of novel [1,2,4]triazolo[1,5-b][1,2,4,5]tetrazines and investigation of their fungistatic activityen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3762/bjoc.18.29-
dc.identifier.scopus85128396407-
local.contributor.employeeKorotina, A.V., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federationen
local.contributor.employeeTolshchina, S.G., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federationen
local.contributor.employeeIshmetova, R.I., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federationen
local.contributor.employeeEvstigneeva, N.P., Experimental Laboratory Department, Ural Research Institute of Dermatovenerology and Immunopathology, Shcherbakova str. 8, Yekaterinburg, 620076, Russian Federationen
local.contributor.employeeGerasimova, N.A., Experimental Laboratory Department, Ural Research Institute of Dermatovenerology and Immunopathology, Shcherbakova str. 8, Yekaterinburg, 620076, Russian Federationen
local.contributor.employeeZilberberg, N.V., Experimental Laboratory Department, Ural Research Institute of Dermatovenerology and Immunopathology, Shcherbakova str. 8, Yekaterinburg, 620076, Russian Federationen
local.contributor.employeeKungurov, N.V., Experimental Laboratory Department, Ural Research Institute of Dermatovenerology and Immunopathology, Shcherbakova str. 8, Yekaterinburg, 620076, Russian Federationen
local.contributor.employeeRusinov, G.L., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federation, Institute of Chemical Engineering, Ural Federal University named after the first President of Russia B. N. Yeltsin, Mira str. 19, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeChupakhin, O.N., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federation, Institute of Chemical Engineering, Ural Federal University named after the first President of Russia B. N. Yeltsin, Mira str. 19, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeCharushin, V.N., Laboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federation, Institute of Chemical Engineering, Ural Federal University named after the first President of Russia B. N. Yeltsin, Mira str. 19, Yekaterinburg, 620002, Russian Federationen
local.description.firstpage243-
local.description.lastpage250-
local.volume18-
dc.identifier.wos000767283000001-
local.contributor.departmentLaboratory of Heterocyclic Compounds, Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch, S. Kovalevskaya str. 22/20, Yekaterinburg, 620108, Russian Federationen
local.contributor.departmentExperimental Laboratory Department, Ural Research Institute of Dermatovenerology and Immunopathology, Shcherbakova str. 8, Yekaterinburg, 620076, Russian Federationen
local.contributor.departmentInstitute of Chemical Engineering, Ural Federal University named after the first President of Russia B. N. Yeltsin, Mira str. 19, Yekaterinburg, 620002, Russian Federationen
local.identifier.pure29832560-
local.identifier.eid2-s2.0-85128396407-
local.identifier.wosWOS:000767283000001-
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