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dc.contributor.authorNagarjuna, U.en
dc.contributor.authorSravya, G.en
dc.contributor.authorDurgamma, S.en
dc.contributor.authorPadmaja, A.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2021-08-31T15:00:11Z-
dc.date.available2021-08-31T15:00:11Z-
dc.date.issued2019-
dc.identifier.citationSynthesis of a new class of heteroaryl dipyrazolyl carbothioamides and heteroaryl dipyrazolyl thiazoles and evaluation as antioxidants / U. Nagarjuna, G. Sravya, S. Durgamma, et al. — DOI 10.1063/1.5087371 // AIP Conference Proceedings. — 2019. — Vol. 2063. — 040039.en
dc.identifier.isbn9780735417915-
dc.identifier.issn0094243X-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85060474484&doi=10.1063%2f1.5087371&partnerID=40&md5=a8eff6499398760d9d56fca753b8790d
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/76541/1/978-5-7996-2691-4_196.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/101847-
dc.description.abstractA new class of indolyl dipyrazoles and indolyl dipyrazolyl thiazoles were prepared from the Michael acceptor (E)-3-(1H-indol-3-yl)-1-(4-aryl-1H-pyrazol-3-yl)prop-2-en-1-one under ultrasonication. All the compounds were obtained in higher yields and in shorter reaction times under ultrasound irradiation method. The lead compounds were tested for antioxidant activity. Amongst all the tested compounds methoxy substituted indolyl dipyrazolyl thiazole displayed pronounced antioxidant activity. © 2019 Author(s).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherAmerican Institute of Physics Inc.en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceAIP Conf. Proc.2
dc.sourceAIP Conference Proceedingsen
dc.titleSynthesis of a new class of heteroaryl dipyrazolyl carbothioamides and heteroaryl dipyrazolyl thiazoles and evaluation as antioxidantsen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/1.5087371-
dc.identifier.scopus85060474484-
local.contributor.employeeNagarjuna, U., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517 502, India
local.contributor.employeeSravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeDurgamma, S., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517 502, India
local.contributor.employeePadmaja, A., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517 502, India
local.contributor.employeeZyryanov, G.V., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation, I. Ya.Postovskiy Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, 22 S. Kovalevskoy Street, Yekaterinburg, 620219, Russian Federation
local.volume2063-
dc.identifier.wos000598565200064-
local.contributor.departmentDepartment of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517 502, India
local.contributor.departmentUral Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.departmentI. Ya.Postovskiy Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, 22 S. Kovalevskoy Street, Yekaterinburg, 620219, Russian Federation
local.identifier.puredce7757d-6d09-4421-a610-9b224e58d194uuid
local.identifier.pure8867528-
local.description.order040039-
local.identifier.eid2-s2.0-85060474484-
local.identifier.wosWOS:000598565200064-
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