Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/101846
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dc.contributor.authorTeja, G. L.en
dc.contributor.authorSankar, P. S.en
dc.contributor.authorReddy, N. B.en
dc.contributor.authorPadmavathi, V.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 and antimicrobial activity of spiroheterocycles / G. L. Teja, P. S. Sankar, N. B. Reddy, et al. — DOI 10.1063/1.5087391 // AIP Conference Proceedings. — 2019. — Vol. 2063. — 040059.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-s2.0-85060477790&doi=10.1063%2f1.5087391&partnerID=40&md5=dd8f80dfad424627daac956a0bd5f9ec
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/76533/1/978-5-7996-2691-4_189.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/101846-
dc.description.abstractA new class of spiroheterocycles-pyrazolinyl thienofuranones and isoxazolinyl thienofuranones were prepared from benzylidene thienofuranones by 1,3-dipolar cycloaddition of nitrile imines and nitrile oxides. The dipolar reagents were generated from araldehyde phenylhydrazones and araldoximes in the presence of phase transfer catalyst. All the compounds are tested for their antimicrobial activity. Chloro substituted pyrazolinyl and isoxazolinyl thienofuranones displayed prominent antibacterial activity against B. subtilis greater than the standard drug Chloramphenicol and antifungal activity against A. niger greater than Ketoconazole. © 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 and antimicrobial activity of spiroheterocyclesen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/1.5087391-
dc.identifier.scopus85060477790-
local.contributor.employeeTeja, G.L., Department of Chemistry, Sri Venkateswara University, Tirupati, A. P., 517 502, India
local.contributor.employeeSankar, P.S., Department of Chemistry, Sri Venkateswara University, Tirupati, A. P., 517 502, India
local.contributor.employeeReddy, N.B., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeePadmavathi, V., 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.wos000598565200084-
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.pure49f60034-5b65-4686-a16f-17c25b5ab8b5uuid
local.identifier.pure8867853-
local.description.order040059-
local.identifier.eid2-s2.0-85060477790-
local.identifier.wosWOS:000598565200084-
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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