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Synthesis of new xanthone derivatives

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2011-02-22T20:47:16Z
dc.date.available2011-02-22T20:47:16Z
dc.date.issued2005
dc.description.abstractXanthones are a class of heterocyclic compounds widely distributed in the plant kingdom (1). Since a long time ago, compounds with the xanthone core are of great interest for chemists, biologists and pharmacologists due to their potencial biological properties. Certain natural and synthetic derivatives have shown important anti-fungal, anti-tumour, anti-inflammatory as well as antioxidant activities (1 ,2).
dc.identifier.citationSantos, Clementina M.M.; Silva, Artur; Cavaleiro, José (2005). Synthesis of new xanthone derivatives. In XXth International Colloquim on Heterocyclic Chemistry. Palermopor
dc.identifier.urihttp://hdl.handle.net/10198/3491
dc.language.isoengpor
dc.relationStudy of the reactivity and transformations of styrylchromones and related compounds
dc.titleSynthesis of new xanthone derivativespor
dc.typeconference object
dspace.entity.typePublication
oaire.awardTitleStudy of the reactivity and transformations of styrylchromones and related compounds
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCTI%2FQUI%2F38394%2F2001/PT
oaire.citation.conferencePlacePalermo, Itáliapor
oaire.citation.titleXXth International Colloquim on Heterocyclic Chemistrypor
oaire.fundingStreamPOCI
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.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isProjectOfPublication1e2fd672-e449-42cb-b1b2-37019185155d
relation.isProjectOfPublication.latestForDiscovery1e2fd672-e449-42cb-b1b2-37019185155d

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