Publication
A novel route for the synthesis of 2,3-Diarylxanthones
dc.contributor.author | Santos, Clementina M.M. | |
dc.contributor.author | Silva, Artur | |
dc.contributor.author | Cavaleiro, José | |
dc.date.accessioned | 2011-02-16T16:08:40Z | |
dc.date.available | 2011-02-16T16:08:40Z | |
dc.date.issued | 2006 | |
dc.description.abstract | Chemically, 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.citation | Santos, 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. Tessalónica | por |
dc.identifier.uri | http://hdl.handle.net/10198/3427 | |
dc.language.iso | eng | por |
dc.peerreviewed | yes | por |
dc.title | A novel route for the synthesis of 2,3-Diarylxanthones | por |
dc.type | conference object | |
dspace.entity.type | Publication | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/POCI/POCI%2FQUI%2F59284%2F2004/PT | |
oaire.citation.conferencePlace | Tessalónica, Grécia | por |
oaire.citation.title | 4th Eurasian Meeting on Heterocyclic Chemistry | por |
oaire.fundingStream | POCI | |
person.familyName | Santos | |
person.givenName | Clementina M.M. | |
person.identifier.ciencia-id | 9018-DB9C-C590 | |
person.identifier.orcid | 0000-0003-4380-7990 | |
person.identifier.scopus-author-id | 7201458663 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
rcaap.rights | openAccess | por |
rcaap.type | conferenceObject | por |
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