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Novel Hydroxy-9H-xanthen-9-ones derivatives: synthesis and bioactive properties

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2011-09-26T08:56:49Z
dc.date.available2011-09-26T08:56:49Z
dc.date.issued2011
dc.description.abstract9H-Xanthen-9-ones commonly referred as xanthones are a large group of natural heterocyclic compounds with significant bioactive properties (e.g. anti-inflammatory, antibacterial, antimalarial, cytotoxicity and radical scavenging activity).1 In order to explore some of these biological assessments, we developed two methodologies for the synthesis of novel hydroxylated 2,3-diarylxanthone derivatives. The first synthetic route is based on the Heck reaction of the 3-bromochromone 2 followed by aldol condensation and electrocyclisation/oxidation processes to afford the 2,3-diaryl-9H-xanthen-9-ones 1. An efficient and more general approach is the Heck reaction of 3-bromo-2-styrylchromones 3 with styrenes as olefins followed by the in situ electrocyclisation/oxidation processes.2 Pharmacological studies involving the hydroxy-9H-xanthen-9-ones 1,3 which are obtained after cleavage of the methyl group, will also be presented and discussed.por
dc.identifier.citationSantos, Clementina M.M.; Silva, Artur; Cavaleiro, José (2011). Novel Hydroxy-9H-xanthen-9-ones derivatives: synthesis and bioactive properties. In 23rd Internacional Congress on Heterocyclic Chemistry. Glasgowpor
dc.identifier.urihttp://hdl.handle.net/10198/6162
dc.language.isoengpor
dc.titleNovel Hydroxy-9H-xanthen-9-ones derivatives: synthesis and bioactive propertiespor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceGlasgow, Escóciapor
oaire.citation.title23rd International Congress on Heterocyclic Chemistrypor
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0

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