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A novel route for the synthesis of 2,3-Diarylxanthones

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2011-02-16T16:08:40Z
dc.date.available2011-02-16T16:08:40Z
dc.date.issued2006
dc.description.abstractChemically, xanthones are oxygenated heterocyclic compounds with a dibenzo-け-pirone nucleus [1]. Natural derivatives have several types of substituents in different positions of their nucleus, which can be associated to the pharmacological properties presented by this class of compounds [2]. Xanthones bearing aryl substituents are scarce and no natural derivatives have been reported with the 2,3-diaryl substitution pattern. Recently, we have reported the synthesis of several 2,3-diarylxanthones, starting from 3-bromo-2-methylchromone.por
dc.identifier.citationSantos, Clementina M.M.; Silva, Artur; Cavaleiro, José (2006). A novel route for the synthesis of 2,3-Diarylxanthones. In 4th Eurasian Meeting on Heterocyclic Chemistry. Tessalónicapor
dc.identifier.urihttp://hdl.handle.net/10198/3427
dc.language.isoengpor
dc.peerreviewedyespor
dc.titleA novel route for the synthesis of 2,3-Diarylxanthonespor
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCI%2FQUI%2F59284%2F2004/PT
oaire.citation.conferencePlaceTessalónica, Gréciapor
oaire.citation.title4th Eurasian Meeting 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.isProjectOfPublication1a77f25c-e459-4679-93cb-48bc8c6709ac
relation.isProjectOfPublication.latestForDiscovery1a77f25c-e459-4679-93cb-48bc8c6709ac

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