Radical Cyclization of Trichloroacetamides: Synthesis of Lactams

dc.contributor.authorCoussanes, Guilhem
dc.contributor.authorVila, X.
dc.contributor.authorDiaba, Faïza
dc.contributor.authorBonjoch i Sesé, Josep
dc.date.accessioned2018-02-12T14:55:59Z
dc.date.available2018-02-12T14:55:59Z
dc.date.issued2017-01
dc.date.updated2018-02-12T14:55:59Z
dc.description.abstractTrichloroacetamides can act as radical precursors to synthesize nitrogen-containing heterocycles in a variety of processes, mainly involving atom transfer radical cyclizations (ATRC), mediated by Cu(I) or Ru(II) catalysts, and the hydride reductive method, employing either Bu3SnH or (Me3Si)3SiH, or recently NaBH3CN. Additionally, amine-mediated single-electron transfer cyclizations, as well as radical processes promoted by Ni, Fe, Mn, Ti, and Ag, have been developed.
dc.format.extent19 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec667665
dc.identifier.issn0039-7881
dc.identifier.urihttps://hdl.handle.net/2445/119757
dc.language.isoeng
dc.publisherGeorg Thieme Verlag Stuttgart · New York
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1055/s-0036-1588383
dc.relation.ispartofSynthesis, 2017, vol. 49, num. 07, p. 1481-1499
dc.relation.urihttps://doi.org/10.1055/s-0036-1588383
dc.rightscc-by-nc-nd (c) Coussanes, G. et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject.classificationLactames
dc.subject.classificationHidrurs
dc.subject.otherLactams
dc.subject.otherHydrides
dc.titleRadical Cyclization of Trichloroacetamides: Synthesis of Lactams
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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