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dc.creatorÁlvarez Casao, Yolandaes
dc.creatorEstepa, Beatrizes
dc.creatorMonge Fernández, Davides
dc.creatorRos, Abeles
dc.creatorIglesias Sigüenza, Francisco Javieres
dc.creatorÁlvarez, Eleuterioes
dc.creatorFernández Fernández, Rosario Fátimaes
dc.creatorLassaletta, José M.es
dc.date.accessioned2022-11-10T17:53:03Z
dc.date.available2022-11-10T17:53:03Z
dc.date.issued2016
dc.identifier.citationÁlvarez Casao, Y., Estepa, B., Monge Fernández, D., Ros, A., Iglesias Sigüenza, F.J., Álvarez, E.,...,Lassaletta, J.M. (2016). Pyridine–hydrazone ligands in enantioselective palladium-catalyzed Suzuki–Miyaura cross-couplings. Tetrahedron, 72 (34), 5184-5190. https://doi.org/10.1016/j.tet.2015.12.053.
dc.identifier.issn0040-4020es
dc.identifier.issn1464-5416es
dc.identifier.urihttps://hdl.handle.net/11441/139270
dc.description.abstractThe geometries and coordination properties of modular pyridineehydrazone N,N-ligands containing C2- symmetric trans-2,5-diphenylpyrrolidine and trans-2,5-diphenylpiperidine as the terminal dialkylamino units have been analyzed by X-ray diffraction analysis of [PdCl2(N,N)] complexes [(N,N)¼pyridine hy- drazone ligand]. In combination with Pd(OAc)2 as the precatalyst, these ligands provide high enantio- selectivities (up to 95:5 er) in asymmetric SuzukieMiyaura cross couplings of 2-methoxy-1-naphthyl bromides with 1-naphthyl and 2-tolyl boronic acids.es
dc.description.sponsorshipMinisterio de Economía y Competitividad TQ2013-48164-C2-1-P, CTQ2013- 48164-C2-2-P, CTQ2014-51912-REDC, RYC-2013-12585es
dc.description.sponsorshipJunta de Andalucía 2012/FQM 1078es
dc.formatapplication/pdfes
dc.format.extent7 p.es
dc.language.isoenges
dc.publisherElsevieres
dc.relation.ispartofTetrahedron, 72 (34), 5184-5190.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCross-couplinges
dc.subjectN-Ligandses
dc.subjectAsymmetric catalysises
dc.subjectPalladiumes
dc.subjectBiarylses
dc.titlePyridine–hydrazone ligands in enantioselective palladium-catalyzed Suzuki–Miyaura cross-couplingses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química orgánicaes
dc.relation.projectIDTQ2013-48164-C2-1-Pes
dc.relation.projectIDCTQ2013- 48164-C2-2-Pes
dc.relation.projectIDCTQ2014-51912-REDCes
dc.relation.projectIDRYC-2013-12585es
dc.relation.projectID2012/FQM 1078es
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tet.2015.12.053es
dc.identifier.doi10.1016/j.tet.2015.12.053es
dc.journaltitleTetrahedrones
dc.publication.volumen72es
dc.publication.issue34es
dc.publication.initialPage5184es
dc.publication.endPage5190es
dc.contributor.funderMinisterio de Economía y Competitividad (MINECO). Españaes
dc.contributor.funderJunta de Andalucíaes

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