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dc.contributor.authorSravya, G.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorRamaseshaiah, K.en
dc.contributor.authorMallikarjuna Reddy, G.en
dc.contributor.authorSuresh, Reddy, C.en
dc.contributor.authorBakthavatchala Reddy, N.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2020-09-29T09:46:24Z-
dc.date.available2020-09-29T09:46:24Z-
dc.date.issued2019-
dc.identifier.citationA concise and efficient synthesis of an impurity, N-desmethyl alcaftadine from alcaftadine: An H1 antagonist / G. Sravya, G. V. Zyryanov, K. Ramaseshaiah, G. Malli Karjuna Reddy, et al. . — DOI 10.14233/ajchem.2019.22059 // Asian Journal of Chemistry. — 2019. — Vol. 10. — Iss. 31. — P. 2257-2260.en
dc.identifier.issn0970-7077-
dc.identifier.otherhttps://doi.org/10.14233/ajchem.2019.22059pdf
dc.identifier.other1good_DOI
dc.identifier.otherda9876ed-c351-445c-b69e-e253537b58a2pure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85071497704m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/90202-
dc.description.abstractHerein, a simple approach for the synthesis of N-desmethyl alcaftadine, an H1 histamine antagonist in solid state and its structure is presented. The reactions were performed under mild and metal free conditions at reflux temperature within a range of 65-70 ºC and the desired product N-desmethyl alcaftadine was obtained in high purity with good yield (96.42 %). It was detected by ultra-high-performance liquid chromatography (UHPLC). © 2019 Chemical Publishing Co.. All rights reserved.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherChemical Publishing Co.en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceAsian Journal of Chemistryen
dc.subjectALCAFTADINEen
dc.subjectANTIHISTAMINEen
dc.subjectN-DESMETHYL ALCAFTADINEen
dc.titleA concise and efficient synthesis of an impurity, N-desmethyl alcaftadine from alcaftadine: An H1 antagonisten
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.14233/ajchem.2019.22059-
dc.identifier.scopus85071497704-
local.affiliationUral Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federationen
local.affiliationI. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationen
local.affiliationRajeev Gandhi Memorial College of Engineering and Technology (Autonomous), Nandyal, 518501, Indiaen
local.affiliationDepartment of Chemistry, Krishna University, Machilipatnam, 521001, Indiaen
local.affiliationDepartment of Chemistry, Sri Venkateswara University, Tirupati, 517502, Indiaen
local.contributor.employeeSravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeZyryanov, G.V., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovskiy Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, Yekaterinburg, 620219, Russian Federationru
local.contributor.employeeRamaseshaiah, K., Rajeev Gandhi Memorial College of Engineering and Technology (Autonomous), Nandyal, 518501, India, Department of Chemistry, Krishna University, Machilipatnam, 521001, Indiaru
local.contributor.employeeMalli Karjuna Reddy, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeSuresh Reddy, C., Department of Chemistry, Sri Venkateswara University, Tirupati, 517502, Indiaru
local.contributor.employeeBakthavatchala Reddy, N., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federationru
local.description.firstpage2257-
local.description.lastpage2260-
local.issue31-
local.volume10-
local.identifier.pure10767360-
local.identifier.eid2-s2.0-85071497704-
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