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A Novel Short-Step Synthesis of New Xanthenedione Derivatives from the Cyclization of 3-Cinnamoyl-2-styrylchromones

dc.contributor.authorPinto, Diana C. G. A.
dc.contributor.authorSeca, Ana M. L.
dc.contributor.authorLeal, Stephanie B.
dc.contributor.authorSilva, Artur M. S.
dc.contributor.authorCavaleiro, José A. S.
dc.date.accessioned2014-03-28T17:42:43Z
dc.date.available2014-03-28T17:42:43Z
dc.date.issued2011
dc.date.updated2014-03-27T21:19:36Z
dc.description.abstractNovel (E)-3-aryl-4-benzylidene-8-hydroxy-3,4-dihydro-1 H-xanthene-1,9(2H)-diones are prepared by the cyclization of (E,E)-3-cinnamoyl-5-hydroxy-2-styrylchromones efficiently catalyzed with boron tribromide. The (E,E)-3-cinnamoyl-5-hydroxy-2-styrylchromones are obtained from the Baker–Venkataraman rearrangement of (E,E)-2-acetyl-1,3-phenylene bis(3-phenylacrylate), which is greatly improved under microwave irradiation.en
dc.identifier.citationPinto, Diana; Seca, Ana; Leal, Stéphanie; Silva, Artur; Cavaleiro, José (2011). "A Novel Short-Step Synthesis of New Xanthenedione Derivatives from the Cyclization of 3-Cinnamoyl-2-styrylchromones", Synlett, 2011, 14, 2005-2008. http://dx.doi.org/10.1055/s-0030-1261172.en
dc.identifier.issn0936-5214 (Print)
dc.identifier.issn1437-2096 (Online)
dc.identifier.urihttp://hdl.handle.net/10400.3/2927
dc.language.isoengpor
dc.publisherGeorg Thieme Verlagen
dc.relation.publisherversionhttp://dx.doi.org/10.1055/s-0030-1261172por
dc.subjectXanthenedionespor
dc.subject3-Cinnamoyl-5-Hydroxy-2-Styrylchromonespor
dc.subjectMicrowave Irradiationen
dc.subjectCyclizationen
dc.subjectBoron Tribroen
dc.titleA Novel Short-Step Synthesis of New Xanthenedione Derivatives from the Cyclization of 3-Cinnamoyl-2-styrylchromonesen
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage2008por
oaire.citation.startPage2005por
oaire.citation.titleSynlettpor
oaire.citation.volume14por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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