Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/101795
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dc.contributor.authorRasputin, N. A.en
dc.contributor.authorDemina, N. S.en
dc.contributor.authorIrgashev, R. A.en
dc.contributor.authorShchepochkin, A. V.en
dc.contributor.authorRusinov, G. L.en
dc.contributor.authorChupakhin, O. N.en
dc.contributor.authorCharushin, V. N.en
dc.date.accessioned2021-08-31T14:59:52Z-
dc.date.available2021-08-31T14:59:52Z-
dc.date.issued2020-
dc.identifier.citationSynthesis, photophysical and redox properties of the 2,5,7-tri(het)aryl- [1,2,4]triazolo[1,5-a]pyrimidines / N. A. Rasputin, N. S. Demina, R. A. Irgashev, et al. — DOI 10.24820/ARK.5550190.P011.247 // Arkivoc. — 2020. — Vol. 2020. — Iss. 6. — P. -.en
dc.identifier.issn15517004-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85094152481&doi=10.24820%2fARK.5550190.P011.247&partnerID=40&md5=0d34d5d0a8c4f31e0b7eeef1f58af3c0
dc.identifier.urihttp://hdl.handle.net/10995/101795-
dc.description.abstractA number of Y-type push-pull compounds based on the [1,2,4]triazolo[1,5-a]pyrimidine core, namely 5,7- di(het)aryl-substituted 2-phenyl-[1,2,4]triazolo[1,5-a]pyrimidines, were obtained by transition metal free nucleophilic C-H functionalization. Substituents at both the C-5 and C-7 positions were introduced by successive treatment of the starting 6-bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine with Grignard reagents. In addition, the optical and electrochemical properties of the synthesized push-pull systems were studied. © 2020 Arkat. All rights reserved.en
dc.description.sponsorshipThis research study was supported financially by the Russian Science Foundation (Project No. 19-13-00234).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherArkaten
dc.relationinfo:eu-repo/grantAgreement/RSF//19-13-00231en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceArkivoc2
dc.sourceArkivocen
dc.subjectDIRECT (HET)ARYLATIONen
dc.subjectGRIGNARD REAGENTSen
dc.subjectNUCLEOPHILIC AROMATIC SUBSTITUTION OF HYDROGEN (SNH)en
dc.subject[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINEen
dc.titleSynthesis, photophysical and redox properties of the 2,5,7-tri(het)aryl- [1,2,4]triazolo[1,5-a]pyrimidinesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.24820/ARK.5550190.P011.247-
dc.identifier.scopus85094152481-
local.contributor.employeeRasputin, N.A., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeDemina, N.S., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeIrgashev, R.A., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeShchepochkin, A.V., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation
local.contributor.employeeRusinov, G.L., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeChupakhin, O.N., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.contributor.employeeCharushin, V.N., Postovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation, Ural Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.issue6-
local.volume2020-
local.contributor.departmentPostovsky Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, S. Kovalevskaya Str., 22, Ekaterinburg, 620990, Russian Federation
local.contributor.departmentUral Federal University, Mira St. 19, Ekaterinburg, 620002, Russian Federation
local.identifier.pure20125521-
local.identifier.pure836416af-929e-4171-9462-13f3fffc1ea9uuid
local.identifier.eid2-s2.0-85094152481-
local.fund.rsf19-13-00231-
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