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Synthesis of (E)-2-(4-Arylbut-1-en-3-ynyl)-4H-chromen-4-ones

dc.contributor.authorAlbuquerque, Hélio
dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.contributor.authorCavaleiro, José
dc.date.accessioned2014-03-11T14:21:33Z
dc.date.available2014-03-11T14:21:33Z
dc.date.issued2013
dc.description.abstractChromones are a well-known class of naturally occurring oxygencontaining heterocyclic compounds; many of them playing important biological functions in nature [1]. Although 2-methylchromones are one of the scarcest classes of natural chromones, their synthesis and reactivity is well studied. They can participate in several chemical transformations such as oxidation, thiation, hydrogenation, photolysis, cycloaddition and condensation reactions, being useful targets in the synthesis of novel heterocyclic compounds [2]. The acidity of the 2- methyl group, due to the low electron density at C-2 caused by oxygen atom and the α,β-unsaturated ketone system, led us to explore the condensation of 2-methylchromones [3] with propargyl aldehydes [4].por
dc.description.sponsorshipUniversity of Aveiro, Fundação para a Ciência e Tecnologia (FCT, Portugal), European Union, QREN, FEDER and COMPETE for funding the QOPNA Research Unit (project PEst-C/QUI/UI0062/2011) and the Portuguese National NMR Network. Hélio Albuquerque also thanks FCT for his fellowship (SFRH/BI/51556/2011).por
dc.identifier.citationAlbuquerque, Hélio; Santos, Clementina M. M.; Silva, Artur; Cavaleiro, José A. S. (2013). Synthesis of (E)-2-(4-Arylbut-1-en-3-ynyl)-4H-chromen-4-ones. In XXIII Encontro Nacional da Sociedade Portuguesa de Química. Aveiropor
dc.identifier.urihttp://hdl.handle.net/10198/9360
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherUniversidade de Aveiropor
dc.titleSynthesis of (E)-2-(4-Arylbut-1-en-3-ynyl)-4H-chromen-4-onespor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.titleXXIII Encontro Nacional da Sociedade Portuguesa de Químicapor
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0

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