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Efficient access to polysubstituted tetrahydrofurans by electrophilic cyclization of vinylsilyl alcohols
dc.contributor.authorBarbero Pérez, María Asunción 
dc.contributor.authorBarbero San Juan, Héctor 
dc.contributor.authorGonzález Ortega, Alfonso 
dc.contributor.authorPulido Pelaz, Francisco José 
dc.contributor.authorVal, Patricia
dc.contributor.authorDiez de la Varga, Alberto
dc.contributor.authorRodríguez Morán, Joaquín
dc.date.accessioned2024-02-15T15:47:50Z
dc.date.available2024-02-15T15:47:50Z
dc.date.issued2015
dc.identifier.citationRSC Adv., 2015, 5, 49541-49551es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/66278
dc.descriptionProducción Científicaes
dc.description.abstractVinylsilyl alcohols undergo intramolecular cyclization to provide di-, tri- or tetrasubstituted-tetrahydrofurans. The influence of the number and position of substituents in the stereoselectivity of the process has been studied. Moreover, DFT calculations have been performed to get better insight into the influence of the substitution pattern of the vinylsilyl alcohol in the stereoselectivity of the cyclization.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleEfficient access to polysubstituted tetrahydrofurans by electrophilic cyclization of vinylsilyl alcoholses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holderRoyal Society of Chemistryes
dc.identifier.doi10.1039/C5RA06640Aes
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra06640a#!divAbstractes
dc.identifier.publicationfirstpage49541es
dc.identifier.publicationissue61es
dc.identifier.publicationlastpage49551es
dc.identifier.publicationtitleRSC Advanceses
dc.identifier.publicationvolume5es
dc.peerreviewedSIes
dc.description.projectWe thank the Ministry of Education, Culture and Sport (MECD) of Spain (CTQ2009-09302) and the “Junta de Castilla y León” (GR170) for financial support. H.B. and A.D.-V. wish to thank the MECD and “Junta de Castilla y León” for doctorate grants.es
dc.identifier.essn2046-2069es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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