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dc.contributor.authorDíez Poza, Carlos 
dc.contributor.authorBarbero Pérez, María Asunción 
dc.date.accessioned2021-11-08T12:42:38Z
dc.date.available2021-11-08T12:42:38Z
dc.date.issued2021
dc.identifier.citationOrganic Letters, 2021, vol. 23, n. 21. p. 8385-8389es
dc.identifier.issn1523-7060es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/49782
dc.descriptionProducción Científicaes
dc.description.abstractThe silyl-Prins cyclization of geminal vinylsilyl alcohols and aldehydes, promoted by TMSOTf, provides access to polysubstituted tetrahydropyrans in which the silyl group remains in the molecule and an aryl group has migrated from silicon to carbon. This domino silyl-Prins/aryl migration process is general and high-yielding for aryl, vinyl, or alkyl aldehydes. Moreover, cyclization proceeds with very high stereocontrol in a one-pot reaction in which both quaternary and tertiary stereogenic centers have been created.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherACS Publicationses
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classificationAlcoholses
dc.subject.classificationAlcoholeses
dc.subject.classificationAldehydeses
dc.subject.classificationAldehídoses
dc.subject.classificationGeneticses
dc.subject.classificationGenéticaes
dc.subject.classificationCyclizationes
dc.subject.classificationCiclizaciónes
dc.titleUnexpected domino Silyl-Prins/Aryl migration process from geminal Vinylsilyl alcoholses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2021 The Authorses
dc.identifier.doi10.1021/acs.orglett.1c03121es
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.orglett.1c03121es
dc.peerreviewedSIes
dc.description.projectJunta de Castilla y León (project VA294P18)es
dc.description.projectFondo Social Europeo - Junta de Castilla y León (predoctoral grant Q4718001C)es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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