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dc.creatorBarata Vallejo, Sebastian-
dc.creatorBonesi, Sergio Mauricio-
dc.creatorPostigo, Jose Alberto-
dc.date2017-06-08T15:36:59Z-
dc.date2017-06-08T15:36:59Z-
dc.date2015-10-
dc.date2017-06-07T20:44:16Z-
dc.date.accessioned2019-04-29T15:56:06Z-
dc.date.available2019-04-29T15:56:06Z-
dc.identifierBarata Vallejo, Sebastian; Bonesi, Sergio Mauricio; Postigo, Jose Alberto; Photocatalytic fluoroalkylation reactions of organic compounds; Royal Society Of Chemistry; Organic & Biomolecular Chemistry; 13; 40; 10-2015; 11153-11183-
dc.identifier1477-0520-
dc.identifierhttp://hdl.handle.net/11336/17774-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/305699-
dc.descriptionPhotocatalytic methods for fluoroalkyl-radical generation provide more convenient alternatives to the classical perfluoroalkyl-radical (Rf) production through chemical initiators, such as azo or peroxide compounds or the employment of transition metals through a thermal electron transfer (ET) initiation process. The mild photocatalytic reaction conditions tolerate a variety of functional groups and, thus, are handy to the late-stage modification of bioactive molecules. Transition metal-photocatalytic reactions for Rf radical generation profit from the redox properties of coordinatively saturated Ru or Ir organocomplexes to act as both electron donor and reductive species, thus allowing for the utilization of electron accepting and donating fluoroalkylating agents for Rf radical production. On the other hand, laboratory-available and inexpensive photoorgano catalysts (POC), in the absence of transition metals, can also act as electron exchange species upon excitation, resulting in ET reactions that produce Rf radicals. In this work, a critical account of transition metal and transition metal-free Rf radical production will be described with photoorgano catalysts, studying classical examples and the most recent investigations in the field.-
dc.descriptionFil: Barata Vallejo, Sebastian. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina-
dc.descriptionFil: Bonesi, Sergio Mauricio. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina-
dc.descriptionFil: Postigo, Jose Alberto. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina-
dc.formatapplication/pdf-
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dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherRoyal Society Of Chemistry-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/c5ob01486g-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/OB/C5OB01486G#!divAbstract-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectPhotocatalysis-
dc.subjectPerfluoroalkylation-
dc.subjectPhotoorgano catalysis-
dc.subjectMetal catalysis-
dc.subjectQuímica Orgánica-
dc.subjectCiencias Químicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titlePhotocatalytic fluoroalkylation reactions of organic compounds-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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