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Microwave-assisted synthesis of chromeno[3,4-b]xanthones and (benzo[c]cromenyl)chromones

2017Conference poster Open access
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dc.contributor.authorAlbuquerque, Hélio
dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorCavaleiro, José
dc.contributor.authorSilva, Artur
dc.date.accessioned2020-07-20T13:40:22Z
dc.date.available2020-07-20T13:40:22Z
dc.date.issued2017
dc.description.abstractTwo series of novel propargyloxychromones were designed and synthesized. Both chromone derivatives were used as substrates in MW-assisted intramolecular Diels-Alder reactions, affording chromeno[3,4-b]xanthones and (benzo[c]chromenyl)chromones. This is the first report involving chromone derivatives in intramolecular Diels-Alder reactions for the synthesis of new oxygen heterocycles, namely xanthones and flavones.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationAlbuquerque, Hélio; Santos, Clementina M.M.; Cavaleiro, José; Silva, Artur (2017). Microwave-assisted synthesis of chromeno[3,4-b]xanthones and (benzo[c]cromenyl)chromones. In TRAMECH IX - Transmediterranean Colloquium on Heterocyclic Chemistry. Fez, Marrocospt_PT
dc.identifier.urihttp://hdl.handle.net/10198/22492
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectPropargyloxychromonespt_PT
dc.subjectIntramolecular Diels-Alderpt_PT
dc.subjectFlavonespt_PT
dc.subjectXanthonespt_PT
dc.titleMicrowave-assisted synthesis of chromeno[3,4-b]xanthones and (benzo[c]cromenyl)chromonespt_PT
dc.typeconference poster
dspace.entity.typePublication
oaire.citation.conferencePlaceFezpt_PT
oaire.citation.titleTRAMECH IX - Transmediterranean Colloquium on Heterocyclic Chemistrypt_PT
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0

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