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dc.contributor.authorChatterjee, R.en
dc.contributor.authorSarkar, S.en
dc.contributor.authorSantra, S.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorMajee, A.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2021-08-31T15:08:53Z-
dc.date.available2021-08-31T15:08:53Z-
dc.date.issued2020-
dc.identifier.citationBrønsted acidic ionic liquid-catalyzed one-pot synthesis of 4(3 H)-quinazolinones under solvent-free conditions / R. Chatterjee, S. Sarkar, S. Santra, et al. — DOI 10.1063/5.0018520 // AIP Conference Proceedings. — 2020. — Vol. 2280. — 0018520.en
dc.identifier.isbn9780735440104-
dc.identifier.issn0094243X-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85096444077&doi=10.1063%2f5.0018520&partnerID=40&md5=1221154f5eca093caa45caafb5fd96f6
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/80935/1/978-5-6044427-0-8_2019_162.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/103300-
dc.description.abstractA simple, efficient, and green method for the one-pot synthesis of 4(3H)-quinazolinones by condensation of anthranilic acid, orthoesters, and amines in the presence of Brønsted Acidic ionic liquid has been developed. the advantages of the present protocol are this occurred at room temperature, under solvent-free conditions to afford the products in excellent yields, easy workup. © 2020 Author(s).en
dc.description.sponsorshipS. Santra is thankful to the Russian Science Foundation – Russia (ref. # 18-73-00301) for funding.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherAmerican Institute of Physics Inc.en
dc.relationinfo:eu-repo/grantAgreement/RSF//18-73-00301en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceAIP Conf. Proc.2
dc.sourceAIP Conference Proceedingsen
dc.titleBrønsted acidic ionic liquid-catalyzed one-pot synthesis of 4(3 H)-quinazolinones under solvent-free conditionsen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/5.0018520-
dc.identifier.scopus85096444077-
local.contributor.employeeChatterjee, R., Department of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, India
local.contributor.employeeSarkar, S., Department of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, India
local.contributor.employeeSantra, S., Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Street, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeZyryanov, G.V., Department of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Street, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis of Ras (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation
local.contributor.employeeMajee, A., Department of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, India
local.volume2280-
dc.identifier.wos000598468000085-
local.contributor.departmentDepartment of Chemistry, Visva-Bharati (A Central University), Santiniketan, 731235, India
local.contributor.departmentDepartment of Organic and Biomolecular Chemistry, Chemical Engineering Institute, Ural Federal University, 19 Mira Street, Yekaterinburg, 620002, Russian Federation
local.contributor.departmentI. Ya. Postovsky Institute of Organic Synthesis of Ras (Ural Division), 22/20, S. Kovalevskoy/Akademicheskaya St., Yekaterinburg, 62099, Russian Federation
local.identifier.pure3ca73535-9e58-4dc7-bbbe-fb4941904455uuid
local.identifier.pure20121998-
local.description.order18520-
local.identifier.eid2-s2.0-85096444077-
local.fund.rsf18-73-00301-
local.identifier.wosWOS:000598468000085-
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