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Access to indolines from primary phenylethylamines by an unexpected palladium- catalyzed C-H functionalization process

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dc.contributor.authorMancinelli, Andrea
dc.contributor.authorAlbert Mach, Joan
dc.contributor.authorAriza Piquer, Xavier
dc.contributor.authorBarrios Moreno, Leoní Alejandra
dc.contributor.authorGarcía Gómez, Jordi
dc.contributor.authorGómez, Roberto
dc.contributor.authorGranell Sanvicente, Jaime Ramón
dc.date.accessioned2019-09-18T14:54:15Z
dc.date.available2019-09-18T14:54:15Z
dc.date.issued2019-08-29
dc.date.updated2019-09-18T14:54:15Z
dc.description.abstractA new method for the preparation of 2,2-disubstituted indolines from 2-phenylethylamines was developed under Pd catalysis and PhI(OAc)2 as oxidant. Imines derived from 2-pyridinecarboxaldehyde were formed in situ to direct a C-H activation process. The resulting imines were also oxidized to the corresponding amides in the same Pd-catalyzed process to obtain the final indoline as a picolinamide.
dc.format.extent7 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec691245
dc.identifier.issn2046-2069
dc.identifier.urihttps://hdl.handle.net/2445/140436
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1039/C9RA05670J
dc.relation.ispartofRSC Advances, 2019, vol. 9, num. 47, p. 27176-27182
dc.relation.urihttps://doi.org/10.1039/C9RA05670J
dc.rightscc-by (c) Mancinelli, Andrea et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)
dc.subject.classificationPal·ladi (Element químic)
dc.subject.classificationCatàlisi
dc.subject.otherPalladium
dc.subject.otherCatalysis
dc.titleAccess to indolines from primary phenylethylamines by an unexpected palladium- catalyzed C-H functionalization process
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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