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dc.contributor.authorMéndez, Francisco
dc.contributor.authorRichaud, Arlette
dc.contributor.authorAlonso Martín, Julio Alfonso 
dc.date.accessioned2016-12-07T19:00:40Z
dc.date.available2016-12-07T19:00:40Z
dc.date.issued2015
dc.identifier.citationOrganic Letters, 2015, Vol. 17, p. 767 – 769es
dc.identifier.issn1523-7060es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/21481
dc.descriptionProducción Científicaes
dc.description.abstractThe Brønsted–Lowry and Lewis basicity dichotomy in the elimination vs substitution reaction competition is analyzed in terms of a novel Brønsted–Lowry–Lewis basicity ωp/e. This new index unifies the dichotomy and explains the competition between elimination and substitution mechanisms of alkyl centers with para-substituted phenols.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectQuímica analíticaes
dc.titleElimination vs Substitution Reaction. A dicotomy between Bronsted-Lowry and Lewis basicityes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1021/ol5034628es
dc.relation.publisherversionhttp://pubs.acs.org/es
dc.identifier.publicationfirstpage767es
dc.identifier.publicationlastpage769es
dc.identifier.publicationtitleOrganic Letterses
dc.identifier.publicationvolume17es
dc.peerreviewedSIes
dc.description.projectJunta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA050U14)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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