Ruthenium-Catalyzed Heck-Type Alkenylation of Alkyl Bromides

dc.contributor.authorMuñoz Molina, José María
dc.contributor.authorPérez Romero, Pedro José
dc.date.accessioned2019-10-03T08:09:18Z
dc.date.available2019-10-03T08:09:18Z
dc.date.issued2019-05-27
dc.description.abstractThe complex [Cp*RuCl(PPh3)2] displays a high catalytic activity for the Heck-type alkenylation of alkyl bromides, in the first example using this metal under thermal conditions. The coupling reaction proceeds efficiently with a variety of functionalized tertiary, secondary, and primary alkyl bromides. The presence of Hünig’s base has been revealed crucial for this transformation. Preliminary mechanistic studies support the participation of alkyl radicals in the reaction.es_ES
dc.description.centerCIQSO
dc.description.departmentQuímica "Profesor José Carlos Vílchez Martín"
dc.description.sponsorshipWe thank MINECO for a grant (CTQ2017-82893-C2-1-R). We also thank Francisco Molina for X-ray structure determination
dc.identifier.citationMuñoz Molina, J.M., Pérez Romero, P.J.: "Ruthenium-Catalyzed Heck-Type Alkenylation of Alkyl Bromides". Journal of Organic Chemistry. Vol. 84, 12, (2019). https://doi.org/10.1021/acs.joc.9b00898es_ES
dc.identifier.doi10.1021/acs.joc.9b00898
dc.identifier.issn0022-3263
dc.identifier.issn1520-6904 (electrónico)
dc.identifier.urihttp://hdl.handle.net/10272/16747
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/Spanish Ministry of Economy & Competitiveness [CTQ2017-82893-C2-1-R]
dc.relation.publisherversionhttps://doi.org/10.1021/acs.joc.9b00898es_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subject.otherRuthenium catalysises_ES
dc.subject.otherAlkenylationes_ES
dc.subject.otherCross-couplinges_ES
dc.subject.otherSingle electron transferes_ES
dc.subject.otherHomogeneous catalysises_ES
dc.titleRuthenium-Catalyzed Heck-Type Alkenylation of Alkyl Bromideses_ES
dc.typejournal articlees_ES
dc.type.hasVersionAM
dspace.entity.typePublication
relation.isAuthorOfPublication8e141a40-1260-4c0a-a95d-0ef4e63b8aad
relation.isAuthorOfPublicationc6f8222a-d8d2-4736-baa6-4a2330bdf6b6
relation.isAuthorOfPublication.latestForDiscovery8e141a40-1260-4c0a-a95d-0ef4e63b8aad

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