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dc.contributor.authorSravya, G.en
dc.contributor.authorReddy, N. B.en
dc.contributor.authorBalakrishna, A.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2021-08-31T15:00:14Z-
dc.date.available2021-08-31T15:00:14Z-
dc.date.issued2019-
dc.identifier.citationSynthesis and bioassay of styryl sulfonylmethyl oxazolyl tethered morpholines and thiomorpholines / G. Sravya, N. B. Reddy, A. Balakrishna, et al. — DOI 10.1063/1.5087385 // AIP Conference Proceedings. — 2019. — Vol. 2063. — 040053.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-s2.0-85060439268&doi=10.1063%2f1.5087385&partnerID=40&md5=f606c598089b960d4640db15e4c983f9
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/76535/1/978-5-7996-2691-4_190.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/101858-
dc.description.abstractA new class of mono and bis heterocycles- 4-(chloromethyl)-2-((arylethenesulfonyl) methyl)oxazoles and 4- ((2-((arylethenesulfonyl)methyl)oxazol-4-yl)methyl)morpholines/ thiomor- pholines were prepared from the synthetic intermediate arylethenesulfonylacetic acid adopting simple and well versed synthetic methodologies and were studied for their respective antimicrobial activity. The compounds 3c and 6c having chloro substituent on the aromatic ring showed greater antimicrobial activity than those with electron donating groups. All the entitled compounds were characterized by 1H, 13C NMR, mass spectra. © 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 bioassay of styryl sulfonylmethyl oxazolyl tethered morpholines and thiomorpholinesen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/1.5087385-
dc.identifier.scopus85060439268-
local.contributor.employeeSravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeReddy, N.B., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeBalakrishna, A., Rajeev Gandhi Memorial College of Engineering and Technology (Autonomous), Nandyal, Andhra Pradesh, 518501, 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.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.contributor.departmentRajeev Gandhi Memorial College of Engineering and Technology (Autonomous), Nandyal, Andhra Pradesh, 518501, India
local.identifier.pure8861122-
local.identifier.pure4a7493c5-e526-4361-83cb-4a662995028fuuid
local.description.order040053-
local.identifier.eid2-s2.0-85060439268-
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