Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/41859
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dc.contributor.authorMalafaia, Danielapt_PT
dc.contributor.authorSousa, Joana L. C.pt_PT
dc.contributor.authorSilva, Artur M. S.pt_PT
dc.contributor.authorAlbuquerque, Hélio M. T.pt_PT
dc.date.accessioned2024-05-13T16:40:30Z-
dc.date.available2024-05-13T16:40:30Z-
dc.date.issued2023-06-
dc.identifier.urihttp://hdl.handle.net/10773/41859-
dc.description.abstract2-Styrylchromones (2-SCs) are interesting compounds for their biological properties as well as versatility as starting materials for further transformations. Herein, we disclose a new 2-SC derivative—2,2’-[(1E,1’E)-{[hexa-2,4-diyne-1,6-diylbis(oxy)]bis(2,1-phenylene)}bis(ethene-2,1- diyl)]bis(4H-chromen-4-one)—which is a dimeric compound formed by two units of 2-SC linked through a 1,3-diyne moiety. It was obtained in excellent yield (96%) through the copper-catalyzed homocoupling of two molecules of O-propargyl-2-SC. Its structure was unveiled by 1D (1H and 13C) and 2D (HSQC and HMBC) NMR techniques together with HRMS.pt_PT
dc.language.isoengpt_PT
dc.publisherMDPIpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/Concurso de Projetos de I&D em Todos os Domínios Científicos - 2022/2022.06064.PTDC/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/PDQI/2021.05641.BD/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subject2-styrylchromonept_PT
dc.subjectPropargylationpt_PT
dc.subjectCopper catalysispt_PT
dc.subjectTerminal alkyne homocouplingpt_PT
dc.subject1,3-diynept_PT
dc.title2,2’-[(1E,1’E)-{[Hexa-2,4-diyne-1,6-diylbis(oxy)]bis(2,1-phenylene)}bis(ethene-2,1-diyl)]bis(4H-chromen-4-one)pt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue2pt_PT
degois.publication.titleMolbankpt_PT
degois.publication.volume2023pt_PT
dc.identifier.doi10.3390/M1621pt_PT
dc.identifier.essn1422-8599pt_PT
dc.identifier.articlenumberM1621pt_PT
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