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dc.contributor.authorTejedor, David-
dc.contributor.authorDelgado-Hernández, Samuel-
dc.contributor.authorIngold, Mariana-
dc.contributor.authorGarcía-Tellado, Fernando-
dc.date.accessioned2019-06-12T10:42:03Z-
dc.date.available2019-06-12T10:42:03Z-
dc.date.issued2016-10-06-
dc.identifier.citationJournal of Organic Chemistry 81(20): 10099-10105 (2016)-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/10261/183874-
dc.description.abstractA microwave-assisted and base-catalyzed domino manifold to construct 2,4-cyclohexadienone derivatives has been implemented. The domino manifold uses easily accessible tertiary propargyl vinyl ethers bearing a methine group at the homopropargylic position and imidazole as the catalyst to deliver 2,4-cyclohexadienones featuring a key formyl group and a quaternized carbon atom in good yields.-
dc.description.sponsorshipThis research was supported by the Spanish Ministerio de Economía y Competitividad (MINECO) and the European Regional Development Fund (CTQ2015-63894-P) and the Consejo Superior de Investigaciones Científicas (CSIC) (COOPB20088). M.I. thanks the Agencia Nacional de Investigación e Innovación of Uruguay (ANII) for a scholarship.-
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccess-
dc.titleSynthesis of α-Quaternized 2,4-Cyclohexadienones from Propargyl Vinyl Ethers-
dc.typeartículo-
dc.identifier.doi10.1021/acs.joc.6b02137-
dc.relation.publisherversionhttps://doi.org/10.1021/acs.joc.6b02137-
dc.identifier.e-issn1520-6904-
dc.date.updated2019-06-12T10:42:03Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderEuropean Commission-
dc.contributor.funderConsejo Superior de Investigaciones Científicas (España)-
dc.contributor.funderAgencia Nacional de Investigación e Innovación (Uruguay)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008725es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003339es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
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