Publication:
Palladium-Catalyzed Direct Arylations, Alkenylations, and Benzylations through C-H Bond Cleavages with Sulfamates or Phosphates as Electrophiles

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dc.bibliographiccitation.firstpage724
dc.bibliographiccitation.issue4
dc.bibliographiccitation.journalOrganic Letters
dc.bibliographiccitation.lastpage726
dc.bibliographiccitation.volume12
dc.contributor.authorAckermann, Lutz
dc.contributor.authorBarfuesser, Sebastian
dc.contributor.authorPospech, Jola
dc.date.accessioned2018-11-07T08:45:52Z
dc.date.available2018-11-07T08:45:52Z
dc.date.issued2010
dc.description.abstractA catalytic system comprised of Pd(OAc)(2) and bidentate ligand dppe enabled first direct arylations with moisture-stable aryl sulfamates as electrophiles, and proved applicable to unprecedented C-H bond functionalizations with easily accessible alkenyl phosphates as well as benzyl phosphates.
dc.description.sponsorshipDFG
dc.identifier.doi10.1021/ol9028034
dc.identifier.isi000274465900020
dc.identifier.pmid20078115
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/20551
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherAmer Chemical Soc
dc.relation.issn1523-7060
dc.titlePalladium-Catalyzed Direct Arylations, Alkenylations, and Benzylations through C-H Bond Cleavages with Sulfamates or Phosphates as Electrophiles
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dspace.entity.typePublication

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