dc.creatorPostigo, Jose Alberto
dc.date.accessioned2017-05-09T18:29:40Z
dc.date.accessioned2018-11-06T13:25:25Z
dc.date.available2017-05-09T18:29:40Z
dc.date.available2018-11-06T13:25:25Z
dc.date.created2017-05-09T18:29:40Z
dc.date.issued2014-10-15
dc.identifierPostigo, Jose Alberto; Photoinduced perfluorobutylation of organic substrates in aqueous media; Comporter; Biointerface Research in Applied Chemistry; 4; 5; 15-10-2014; 865-872
dc.identifier2069-5837
dc.identifierhttp://hdl.handle.net/11336/16147
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1875205
dc.description.abstractHydroperfluorobutylation of a series of electron-deficient and electron-rich alkenes through consecutive radical reactions employing perfluorobutyl iodide, n-C4F9I, and (Me3Si)3SiH as chain carrier/hydrogen atom donor is described. The photoinduced Halogen Atom Transfer (HAT) reactions of both olefins and alkynes with n-C4F9I are also shown to be achieved efficiently in aqueous mixtures. On the other hand, aromatic and heteroaromatic substrates can be perfluorobutylated with high efficiency in a photoinduced fashion by means of a Homolytic Aromatic Substitution (SHA) process which involves an Electron Transfer (ET) and a Proton Transfer (PT) step.
dc.languageeng
dc.publisherComporter
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://biointerfaceresearch.com/?page_id=829
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPERFLUOROBUTYLATION
dc.subjectRADICAL REACTIONS
dc.subjectPHOTOINDUCED
dc.titlePhotoinduced perfluorobutylation of organic substrates in aqueous media
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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