Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2759
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dc.contributor.authorAksu, Kadir-
dc.contributor.authorOzgeris, Bunyamin-
dc.contributor.authorTumer, Ferhan-
dc.date.accessioned2022-08-17T07:36:06Z-
dc.date.available2022-08-17T07:36:06Z-
dc.date.issued2019-
dc.identifier.urihttp://doi.org/10.25135/acg.oc.55.19.03.1222-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2759-
dc.description.abstractIn this work, new N-substituted 2-aminopyrrole derivatives were synthesized. Initially, some crotonitriles were prepared by condensation of malononitrile with arylmethylketones, which was followed by conversion of them to the bromocrotonitriles. Finally, the synthesis of new N-substituted 2-aminopyrrole derivates were successfully achieved by cyclization of the bromocrotonitriles of (R)-1-phenylethylamine applying Gewald method.en_US
dc.language.isoengen_US
dc.publisherACG PUBLICATIONS, YENIKENT MAHALLESI, FIRAT CADDESI, 1-3, GEBZE-KOCAELI, 41400, TURKEYen_US
dc.relation.isversionof10.25135/acg.oc.55.19.03.1222en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPyrrole; aminopyrrole; Knoevenagel condensation; Gewald reactionen_US
dc.titleSynthesis and characterization of new N-substituted 2-aminopyrrole derivativesen_US
dc.typearticleen_US
dc.relation.journalORGANIC COMMUNICATIONSen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-3783-6501en_US
dc.identifier.volume12en_US
dc.identifier.issue1en_US
dc.identifier.startpage38en_US
dc.identifier.endpage42en_US
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