Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/102911
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dc.contributor.authorDrokin, R. A.en
dc.contributor.authorTiufiakov, D. V.en
dc.contributor.authorVoinkov, E. K.en
dc.contributor.authorSlepukhin, P. A.en
dc.contributor.authorUlomsky, E. N.en
dc.contributor.authorEsaulkova, Y. L.en
dc.contributor.authorVolobueva, A. S.en
dc.contributor.authorLantseva, K. S.en
dc.contributor.authorMisyurina, M. A.en
dc.contributor.authorZarubaev, V. V.en
dc.contributor.authorRusinov, V. L.en
dc.date.accessioned2021-08-31T15:06:10Z-
dc.date.available2021-08-31T15:06:10Z-
dc.date.issued2021-
dc.identifier.citationMethods of Synthesis and Antiviral Activity of New 4-Alkyl-3-Nitro-1,4-Dihydroazolo[5,1-c][1,2,4]Triazin-4-ols / R. A. Drokin, D. V. Tiufiakov, E. K. Voinkov, et al. — DOI 10.1007/s10593-021-02926-2 // Chemistry of Heterocyclic Compounds. — 2021. — Vol. 57. — Iss. 4. — P. 473-478.en
dc.identifier.issn93122-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Bronze, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85105866117&doi=10.1007%2fs10593-021-02926-2&partnerID=40&md5=ffecce64398fdc9606bac8d540eeffec
dc.identifier.otherhttps://link.springer.com/content/pdf/10.1007/s10593-021-02926-2.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/102911-
dc.description.abstract[Figure not available: see fulltext.] An azo coupling reaction of α-nitro ketones with 5-diazoazoles was used to obtain 4-alkyl-3-nitro-1,4-dihydroazolo[5,1-с][1,2,4]triazines, which were characterized with respect to their antiviral activity against influenza and Coxsackie B3 viruses. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.en
dc.description.sponsorshipThis study was funded by the Russian Science Foundation (project No. 20-13-00142).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherSpringeren
dc.relationinfo:eu-repo/grantAgreement/RSF//20-13-00142en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceChem. Heterocycl. Compd.2
dc.sourceChemistry of Heterocyclic Compoundsen
dc.subject3-NITROAZOLO[5,1-С][1,2,4]TRIAZINESen
dc.subjectANTIVIRAL ACTIVITYen
dc.subjectCOXSACKIE B3 VIRUSen
dc.subjectINFLUENZA VIRUSen
dc.subjectTRIAZINESen
dc.subjectΑ-NITRO KETONESen
dc.titleMethods of Synthesis and Antiviral Activity of New 4-Alkyl-3-Nitro-1,4-Dihydroazolo[5,1-c][1,2,4]Triazin-4-olsen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi46106393-
dc.identifier.doi10.1007/s10593-021-02926-2-
dc.identifier.scopus85105866117-
local.contributor.employeeDrokin, R.A., Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeTiufiakov, D.V., Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeVoinkov, E.K., Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeSlepukhin, P.A., Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22/20 Sofyi Kovalevskoi St, Yekaterinburg, 620108, Russian Federation
local.contributor.employeeUlomsky, E.N., Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22/20 Sofyi Kovalevskoi St, Yekaterinburg, 620108, Russian Federation
local.contributor.employeeEsaulkova, Y.L., Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St, Saint Petersburg, 197101, Russian Federation
local.contributor.employeeVolobueva, A.S., Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St, Saint Petersburg, 197101, Russian Federation
local.contributor.employeeLantseva, K.S., Saint Petersburg State University, 7/9 University Embankment, Saint Petersburg, 199034, Russian Federation
local.contributor.employeeMisyurina, M.A., Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St, Saint Petersburg, 197101, Russian Federation
local.contributor.employeeZarubaev, V.V., Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St, Saint Petersburg, 197101, Russian Federation
local.contributor.employeeRusinov, V.L., Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22/20 Sofyi Kovalevskoi St, Yekaterinburg, 620108, Russian Federation
local.description.firstpage473-
local.description.lastpage478-
local.issue4-
local.volume57-
dc.identifier.wos000649250900005-
local.contributor.departmentUral Federal University named after the first President of Russia B. N. Yeltsin, 19 Mira St, Yekaterinburg, 620002, Russian Federation
local.contributor.departmentPostovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22/20 Sofyi Kovalevskoi St, Yekaterinburg, 620108, Russian Federation
local.contributor.departmentSaint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St, Saint Petersburg, 197101, Russian Federation
local.contributor.departmentSaint Petersburg State University, 7/9 University Embankment, Saint Petersburg, 199034, Russian Federation
local.identifier.pure22099283-
local.identifier.pure4143a279-f881-4449-a4b0-231ec86bdd8euuid
local.identifier.eid2-s2.0-85105866117-
local.fund.rsf20-13-00142-
local.identifier.wosWOS:000649250900005-
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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