Mostrar el registro sencillo del ítem

Artículo

dc.creatorRos Lao, Abeles
dc.creatorFernández Fernández, Rosario Fátimaes
dc.creatorLassaletta Simón, José Maríaes
dc.date.accessioned2018-01-09T15:24:44Z
dc.date.available2018-01-09T15:24:44Z
dc.date.issued2014
dc.identifier.citationRos Lao, A., Fernández Fernández, R. y Lassaletta Simón, J.M. (2014). Functional group directed C-H borylation. Chemical Society Reviews, 43, 3229-3243.
dc.identifier.issn1460-4744es
dc.identifier.urihttp://hdl.handle.net/11441/68538
dc.description.abstractThe direct borylation of hydrocarbons via C-H activation has reached an impressive level of sophistication and efficiency, emerging as a fundamental tool in synthesis because of the versatility offered by organoboron compounds. As a remarkable particularity, the catalytic systems originally developed for these reactions are relatively insensitive to directing effects, and the regioselectivity of the borylations is typically governed by steric factors. Likely stimulated by the great synthetic potential of the expected functionalised organoboranes, however, many groups have recently focused on the development of complementary strategies for directed, site-selective borylation reactions where a directing group controls the course of the reaction. In this tutorial review, the different strategies and findings related to the development of these directed borylation reactions via C(sp2)-H or C(sp3)-H activation will be summarized and discussed. © 2014 the Partner Organisations.es
dc.description.sponsorshipMinisterio de Ciencia e Innovación CTQ2010-15297, CTQ2010-14974es
dc.description.sponsorshipJunta de Andalucía 2008/FQM-3833, 2009/FQM-4537es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistry (Great Britain)es
dc.relation.ispartofChemical Society Reviews, 43, 3229-3243.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleFunctional group directed C-H borylationes
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.projectIDCTQ2010-15297es
dc.relation.projectIDCTQ2010-14974es
dc.relation.projectID2008/FQM-3833es
dc.relation.projectID2009/FQM-4537es
dc.relation.publisherversionhttp://dx.doi.org/10.1039/c3cs60418ges
dc.identifier.doi10.1039/c3cs60418ges
idus.format.extent15 p.es
dc.journaltitleChemical Society Reviewses
dc.publication.volumen43es
dc.publication.initialPage3229es
dc.publication.endPage3243es
dc.contributor.funderMinisterio de Ciencia e Innovación (MICIN). España
dc.contributor.funderJunta de Andalucía

FicherosTamañoFormatoVerDescripción
Functional group directed.pdf4.852MbIcon   [PDF] Ver/Abrir  

Este registro aparece en las siguientes colecciones

Mostrar el registro sencillo del ítem

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como: Attribution-NonCommercial-NoDerivatives 4.0 Internacional