1. Электронный научный архив УрФУ
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  3. Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC
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dc.contributor.authorRammohan, A.en
dc.contributor.authorKrinochkin, A. P.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorShtaitz, Y. K.en
dc.contributor.authorSharafieva, E. R.en
dc.contributor.authorGaviko, V. S.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2024-04-05T16:36:43Z-
dc.date.available2024-04-05T16:36:43Z-
dc.date.issued2023-
dc.identifier.citationRammohan, A, Krinochkin, A, Kopchuk, D, Shtaitz, Y, Sharafieva, E, Gaviko, V, Zyryanov, G & Chupakhin, O 2023, 'Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium', Russian Journal of Organic Chemistry, Том. 59, № 9, стр. 1633-1636. https://doi.org/10.1134/S1070428023090233harvard_pure
dc.identifier.citationRammohan, A., Krinochkin, A., Kopchuk, D., Shtaitz, Y., Sharafieva, E., Gaviko, V., Zyryanov, G., & Chupakhin, O. (2023). Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. Russian Journal of Organic Chemistry, 59(9), 1633-1636. https://doi.org/10.1134/S1070428023090233apa_pure
dc.identifier.issn1070-4280-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Hybrid Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85177430543&doi=10.1134%2fS1070428023090233&partnerID=40&md5=15595112e9b59f621225a0e406cfbfef1
dc.identifier.otherhttps://link.springer.com/content/pdf/10.1134/S1070428023090233.pdfpdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130986-
dc.description.abstractAbstract: We previously reported the solvent-free reaction of 5-aryl-3-(pyridin-2-yl)-1,2,4-triazine-5-carbo-nitriles with 2-amino-4-aryl-1,3-oxazoles, which afforded 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles. Similar reaction in anhydrous medium led to the formation of two products, previously described 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles (up to 44%) and 4,5-diaryl-2,2′-bipyridine-6-carbonitriles (up to 32%). © 2023, The Author(s).en
dc.description.sponsorshipCouncil on grants of the President of the Russian Federation: MK-320.2021.1.3en
dc.description.sponsorshipThis study was financially supported by the Council for Grants at the President of the Russian Federation (project no. MK-320.2021.1.3).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherPleiades Publishingen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceRussian Journal of Organic Chemistry2
dc.sourceRussian Journal of Organic Chemistryen
dc.subject2-AMINOOXAZOLESen
dc.subject4,5-DIARYL-3-HYDROXY-2,2′-BIPYRIDINESen
dc.subject5-CYANO-1,2,4-TRIAZINESen
dc.subjectANHYDROUS CONDITIONSen
dc.subjectAZA-DIELS–ALDER REACTIONen
dc.subjectSOLVENT-FREE REACTIONen
dc.titleReaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Mediumen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.rsi63921307-
dc.identifier.doi10.1134/S1070428023090233-
dc.identifier.scopus85177430543-
local.contributor.employeeRammohan, A., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeKrinochkin, A.P., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeeKopchuk, D.S., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeeShtaitz, Y.K., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeSharafieva, E.R., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Ural Medical University, Ministry of Health of the Russian Federation, Yekaterinburg, 620028, Russian Federationen
local.contributor.employeeGaviko, V.S., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Mikheev Institute of Metal Physics, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620108, Russian Federationen
local.contributor.employeeZyryanov, G.V., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.contributor.employeeChupakhin, O.N., Yeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federation, Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.description.firstpage1633-
local.description.lastpage1636-
local.issue9-
local.volume59-
dc.identifier.wos001156603300006-
local.contributor.departmentYeltsin Ural Federal University, Yekaterinburg, 620002, Russian Federationen
local.contributor.departmentPostovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.contributor.departmentUral Medical University, Ministry of Health of the Russian Federation, Yekaterinburg, 620028, Russian Federationen
local.contributor.departmentMikheev Institute of Metal Physics, Ural Branch, Russian Academy of Sciences, Yekaterinburg, 620108, Russian Federationen
local.identifier.pure49311028-
local.identifier.eid2-s2.0-85177430543-
local.identifier.wosWOS:001156603300006-
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