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A novel and efficient route for the syntheses of hydroxylated 2,3-diarylxanthones

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2011-02-02T16:14:15Z
dc.date.available2011-02-02T16:14:15Z
dc.date.issued2007
dc.description.abstractA novel, efficient and general route for the synthesis of hy-droxylated 2,3-diarylxanthones is described. 3-Bromo-2-styrylchromones, the key intermediate of this synthesis, is obtained by a Baker-Venkataraman rearrangement of appropriate 2’-cinnamoyloxyacetophenones, followed by a one-pot reaction with phenyltrimethylammonium tribromide. The Heck reaction of these bromochromones with substituted styrenes gives methoxylated 2,3-diarylxanthones. The cleavage of the methyl groups with BBr3 gives the desired hydroxylated 2,3-diarylxanthones.por
dc.identifier.citationSantos, Clementina; Silva, Artur; Cavaleiro, José (2007). A novel and efficient route for the syntheses of hydroxylated 2,3-diarylxanthones. Synlett. 20, p. 3113-3116por
dc.identifier.doi10.1055/s-2007-990900
dc.identifier.urihttp://hdl.handle.net/10198/3240
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherThieme Verlagpor
dc.subjectHydroxylated diarylxanthonespor
dc.subject3-bromo-2-styrylchromonespor
dc.subjectHeck reactionpor
dc.subjectPhenyltrimethylammonium tribromidepor
dc.subjectDemethylationpor
dc.titleA novel and efficient route for the syntheses of hydroxylated 2,3-diarylxanthonespor
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POCI/POCI%2FQUI%2F59284%2F2004/PT
oaire.citation.endPage3116por
oaire.citation.startPage3113por
oaire.citation.titleSynlettpor
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.typearticlepor
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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