Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/217580
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dc.contributor.authorPuig, Jordi-
dc.contributor.authorBonjoch, Josep-
dc.contributor.authorBradshaw, Ben-
dc.date.accessioned2025-01-16T19:26:47Z-
dc.date.available2025-01-16T19:26:47Z-
dc.date.issued2023-08-30-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://hdl.handle.net/2445/217580-
dc.description.abstractThe use of isocyanides as acceptor groups in metal–hydride hydrogen atom transfer (MHAT) coupling reactions with nonactivated alkenes to form heterocycles is described. Monosubstituted alkenes couple and cyclize directly, whereas more substituted alkenes proceed via a two-step, one-pot procedure involving MHAT reductive cyclization followed by a MHAT Minisci coupling upon the addition of acid. To highlight the utility of the methodology, a diverse variety of substituted heterocycles such as phenanthridines, indoles, and isoquinolines were prepared.-
dc.format.extent5 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1021/acs.orglett.3c02358-
dc.relation.ispartofOrganic Letters, 2023, vol. 25, num.35, p. 6539-6543-
dc.relation.urihttps://doi.org/10.1021/acs.orglett.3c02358-
dc.rightscc by (c) Jordi Puig, et al., 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationHidrogen-
dc.subject.classificationAlquens-
dc.subject.classificationÀtoms-
dc.subject.otherHydrogen-
dc.subject.otherAlkenes-
dc.subject.otherAtoms-
dc.titleIsocyanides as Acceptor Groups in MHAT Reactions with Unactivated Alkenes-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec745439-
dc.date.updated2025-01-16T19:26:47Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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