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Recent developments in the synthesis of novel xanthone-1,2,3-triazole dyads

dc.contributor.authorAlbuquerque, Hélio
dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2016-05-30T14:31:59Z
dc.date.available2016-05-30T14:31:59Z
dc.date.issued2015
dc.description.abstractThe development of multi-target drugs for treating complex multifactorial diseases constitutes an active research ield. This kind of drugs has gained much importance as alternative strategy to combination therapy (“cocktail drugs”).1 A common way to design them brings together two different pharmacophores in one single molecule (so-called dyads). Following this idea and being aware that xanthones2 and 1,2,3-triazoles3 possess important pharmacological properties, we combined these two heterocycles in one molecule to create new dyads with improved therapeutic potential. In this work, new xanthone-1,2,3-triazole dyads were prepared from novel (E)-2-(4-arylbut-1-en-3-yn-1-yl)chromones by two different approaches to evaluate their eficiency and sustainability. Both methodologies involved Diels-Alder reactions to build the xanthone core, which were optimized using microwave irradiation as alternative heating method, and 1,3-dipolar cycloadditions to insert the 1,2,3-triazole moiety (Figure 1).4 All final and intermediate compounds were fully characterized by 1D and 2D NMR techniques.pt_PT
dc.identifier.citationAlbuquerque, Hélio; Santos, Clementina M.M.; Silva, Artur M. S.; Cavaleiro, J. A. S. (2015). Recent developments in the synthesis of novel xanthone-1,2,3-triazole dyads. In 11º Encontro Nacional de Química Orgânica e 4º Encontro de Química Terapêutica. Porto. ISBN 978-989-98541-9-2pt_PT
dc.identifier.isbn978-989-98541-9-2
dc.identifier.urihttp://hdl.handle.net/10198/12948
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleRecent developments in the synthesis of novel xanthone-1,2,3-triazole dyadspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FQUI%2F00062%2F2013/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F86277%2F2012/PT
oaire.citation.conferencePlacePortopt_PT
oaire.citation.title11º Encontro Nacional de Química Orgânica e 4º Encontro de Química Terapêuticapt_PT
oaire.fundingStream5876
oaire.fundingStreamSFRH
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
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relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isProjectOfPublicationa955d531-2af9-40df-baaf-a064d8a697e9
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