Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/101833
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dc.contributor.authorBabu, K. N.en
dc.contributor.authorRekha, T.en
dc.contributor.authorSravya, G.en
dc.contributor.authorReddy, P. R.en
dc.contributor.authorPadmavathi, V.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2021-08-31T15:00:09Z-
dc.date.available2021-08-31T15:00:09Z-
dc.date.issued2019-
dc.identifier.citationSynthesis and antimicrobial activity of bis(azolyl) urea derivatives / K. N. Babu, T. Rekha, G. Sravya, et al. — DOI 10.1063/1.5087354 // AIP Conference Proceedings. — 2019. — Vol. 2063. — 040022.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-s2.0-85060499232&doi=10.1063%2f1.5087354&partnerID=40&md5=a41d20829353924cc165c158938e5c3a
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/76532/1/978-5-7996-2691-4_188.pdfm
dc.identifier.urihttp://hdl.handle.net/10995/101833-
dc.description.abstractA variety of bis(azolyl) urea derivatives were prepared by the reaction of methyl benzazoyl carbamates with azolyl amines in the presence of mild base and studied their antimicrobial activity. The presence of electron donating substituents on the aromatic ring enhanced the activity. Methoxy substituted benzothiazolyl thiazolyl urea, benzothiazolyl imidazolyl urea and benzimidazolyl thiazolyl urea displayed prominent antibacterial activity against Bacillus subtilis. Benzothiazolyl imidazolyl urea and methyl substituted benzimidazolyl imidazolyl urea showed good antifungal activity against Aspergillus niger. © 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 bis(azolyl) urea derivativesen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/1.5087354-
dc.identifier.scopus85060499232-
local.contributor.employeeBabu, K.N., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517502, India
local.contributor.employeeRekha, T., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517502, India
local.contributor.employeeSravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeReddy, P.R., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517502, India
local.contributor.employeePadmavathi, V., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517502, 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-
local.contributor.departmentDepartment of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517502, 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.pure8864631-
local.identifier.pure4d732502-8153-4804-b2e7-5fd151a26f7auuid
local.description.order040022-
local.identifier.eid2-s2.0-85060499232-
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