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Synthesis of benzannelated sultams by intramolecular Pd-catalyzed arylation of tertiary sulfonamides

dc.contributor.authorRassadin, Valentin A
dc.contributor.authorScholz, Mirko
dc.contributor.authorKlochkova, Anastasiia A
dc.contributor.authorde Meijere, Armin
dc.contributor.authorSokolov, Victor V
dc.date.accessioned2019-12-17T13:18:30Z
dc.date.available2019-12-17T13:18:30Z
dc.date.issued2017de
dc.relation.ISSN1860-5397de
dc.identifier.urihttp://resolver.sub.uni-goettingen.de/purl?gs-1/17019
dc.description.abstractA new and efficient approach to five- and six-membered benzannelated sultams by intramolecular C-arylation of tertiary 1-(methoxycarbonyl)methanesulfonamides under palladium catalysis is described. In case of the α-toluenesulfonamide derivative, an unexpected formation of a 2,3-diarylindole was observed under the same conditions.de
dc.language.isoengde
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectarylation; fused-ring systems; indole formation; palladium catalysis; sultamsde
dc.subject.ddc540
dc.titleSynthesis of benzannelated sultams by intramolecular Pd-catalyzed arylation of tertiary sulfonamidesde
dc.typejournalArticlede
dc.identifier.doi10.3762/bjoc.13.187
dc.type.versionpublishedVersionde
dc.relation.eISSN1860-5397
dc.bibliographicCitation.volume13de
dc.bibliographicCitation.firstPage1932de
dc.bibliographicCitation.lastPage1939de
dc.type.subtypejournalArticle
dc.identifier.pmid29062411
dc.description.statuspeerReviewedde
dc.bibliographicCitation.journalBeilstein Journal of Organic Chemistryde


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