Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/101859
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dc.contributor.authorYamini, G.en
dc.contributor.authorSekhar, M. M.en
dc.contributor.authorSravya, G.en
dc.contributor.authorSreenivasulu, T.en
dc.contributor.authorPadmaja, 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.citationGreen approach for the synthesis of some new diamidomethane linked pyridinyl pyrazoles / G. Yamini, M. M. Sekhar, G. Sravya, et al. — DOI 10.1063/1.5087400 // AIP Conference Proceedings. — 2019. — Vol. 2063. — 040068.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-s2.0-85060438565&doi=10.1063%2f1.5087400&partnerID=40&md5=a0dfb87818045cdfcff34b4ca0b6f5c0
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/76506/1/978-5-7996-2691-4_164.pdfm
dc.identifier.urihttp://hdl.handle.net/10995/101859-
dc.description.abstractSome new diamidomethane linked pyridinyl pyrazoles were synthesized adopting green approach by 1,3-dipolar cycloaddition of nitrile imines generated from araldehyde phenylhydrazones in the presence of iodosobenzene and CTAB followed by oxidation with I2 in DMSO. All the compounds were characterized by IR, 1H NMR, 13C NMR, mass and microanalyses. © 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.titleGreen approach for the synthesis of some new diamidomethane linked pyridinyl pyrazolesen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/1.5087400-
dc.identifier.scopus85060438565-
local.contributor.employeeYamini, G., Department of Chemistry, Sri Venkateswara University, Tirupati, A.P., 517 502, India
local.contributor.employeeSekhar, M.M., 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.employeeSreenivasulu, T., 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-
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.pure8861048-
local.identifier.pure679407cd-bee8-4373-9ca1-b8f887840642uuid
local.description.order040068-
local.identifier.eid2-s2.0-85060438565-
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