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New Synthesis of 2,3-Diarylxanthones

2005Journal article Open access
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dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2011-04-04T14:25:40Z
dc.date.available2011-04-04T14:25:40Z
dc.date.issued2005
dc.description.abstractA new synthesis of novel 2,3-diarylxantones is described. This was accomplished by Aldol condensation of 3-bromo-2-methylchromone with benzaldehydes leading to the formation of 3-bromo-2-styrylchromones, followed by Heck reaction with styrenes.por
dc.identifier.citationSantos, Clementina; Silva, Artur; Cavaleiro, José (2005). New synthesis of 2,3-Diarylxanthones. Synlett. ISSN 0936-5214. 20, p. 3095-3098por
dc.identifier.doi10.1055/s-2005-921928
dc.identifier.issn0936-5214
dc.identifier.urihttp://hdl.handle.net/10198/3929
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherThieme Verlagpor
dc.relationStudy of the reactivity and transformations of styrylchromones and related compounds
dc.subjectDiarylxanthonespor
dc.subject2-Styrylchromonespor
dc.subjectHeck reactionpor
dc.subject3-bromo-2-methylchromonespor
dc.subjectElectrocyclisationpor
dc.titleNew Synthesis of 2,3-Diarylxanthonespor
dc.typejournal article
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.endPage3098por
oaire.citation.startPage3095por
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.isProjectOfPublication1e2fd672-e449-42cb-b1b2-37019185155d
relation.isProjectOfPublication.latestForDiscovery1e2fd672-e449-42cb-b1b2-37019185155d

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