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Synthesis of chromone-related pyrazole compounds

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Vera L.M.
dc.contributor.authorSilva, Artur
dc.date.accessioned2020-01-21T16:30:50Z
dc.date.available2020-01-21T16:30:50Z
dc.date.issued2017
dc.description.abstractChromones, six-membered oxygen heterocycles, and pyrazoles, five-membered two-adjacent-nitrogen-containing heterocycles, represent two important classes of biologically active compounds. Certain derivatives of these scaffolds play an important role in medicinal chemistry and have been extensively used as versatile building blocks in organic synthesis. In this context, we will discuss the most relevant advances on the chemistry that involves both chromone and pyrazole rings. The methods reviewed include the synthesis of chromone-pyrazole dyads, synthesis of chromone-pyrazole-fused compounds, and chromones as starting materials in the synthesis of 3(5)-(2-hydroxyaryl)pyrazoles, among others. This review will cover the literature on the chromone and pyrazole dual chemistry and their outcomes in the 21st century.pt_PT
dc.description.sponsorshipThanks are due to University of Aveiro and FCT/MEC for the financial support of the QOPNA research unit (FCT UID/QUI/00062/2013) and CIQ-UP, University of Porto (POCI-01-0145-FEDER-006980; FCT: UID/QUI/00081/2013) through national founds and, where applicable, co-financed by the FEDER, within the PT2020 Partnership Agreement, as well as to the Polytechnic Institute of Bragança. V.L.M.S. is grateful to FCT for her grant (SFRH/BPD/108807/2015), in the ambit of “QREN e POCH e Tipologia 4.1 e Formação Avançada”, co-sponsored by FSE and by national funds of MCTES.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSantos, Clementina M.M.; Silva, Vera L.M.; Silva, Artur (2017). Synthesis of chromone-related pyrazole compounds. Molecules. ISSN 1420-3049. 22:10, p. 1-47pt_PT
dc.identifier.doi10.3390/molecules22101665pt_PT
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10198/20460
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectAntineoplastic agentspt_PT
dc.subjectChromonespt_PT
dc.subjectDrug designpt_PT
dc.subjectHumanspt_PT
dc.subjectMolecular structurept_PT
dc.subjectPyrazolespt_PT
dc.subjectStructure-activity relationshippt_PT
dc.titleSynthesis of chromone-related pyrazole compoundspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FQUI%2F00062%2F2013/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FQUI%2F00081%2F2013/PT
oaire.citation.issue10pt_PT
oaire.citation.titleMoleculespt_PT
oaire.citation.volume22pt_PT
oaire.fundingStream5876
oaire.fundingStream5876
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.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isProjectOfPublicationa955d531-2af9-40df-baaf-a064d8a697e9
relation.isProjectOfPublicationa230007a-fba4-4e84-ae0b-c8e67df51b68
relation.isProjectOfPublication.latestForDiscoverya230007a-fba4-4e84-ae0b-c8e67df51b68

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