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dc.creatorBožinović, Nina S.
dc.creatorŠolaja, Bogdan A.
dc.creatorOpsenica, Igor
dc.date.accessioned2018-11-22T00:37:29Z
dc.date.available2018-11-22T00:37:29Z
dc.date.issued2016
dc.identifier.issn0352-5139
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/2354
dc.description.abstractA novel and efficient route has been developed to afford dipyridoazepine derivatives from primary amines and 3,3'-(Z)-ethene-1,2-diylbis(4-chloropyridine). The procedure based on a double nucleophilic aromatic substitution provides a valuable synthetic tool for the synthesis of dipyridoazepines. The reaction proceeds without catalyst, under microwave irradiation conditions.en
dc.publisherSerbian Chemical Soc, Belgrade
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172008/RS//
dc.relationSerbian Academy of Sciences and Arts
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of the Serbian Chemical Society
dc.subjectazepinesen
dc.subjectheterocyclesen
dc.subjectnucleophilic aromatic substitutionen
dc.subjecttransition metal-free conditionsen
dc.subjectmicrowave irradiationen
dc.titleMicrowave-assisted synthesis of azepines via nucleophilic aromatic substitutionen
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractШолаја, Богдан A.; Опсеница, Игор; Бозиновиц, Нина;
dc.citation.volume81
dc.citation.issue11
dc.citation.spage1225
dc.citation.epage1230
dc.identifier.wos000388618600001
dc.identifier.doi10.2298/JSC160824074B
dc.citation.other81(11): 1225-1230
dc.citation.rankM23
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3567]
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-84998678147
dc.identifier.fulltexthttps://cherry.chem.bg.ac.rs/bitstream/id/9334/2352.pdf


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