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

dc.contributor.author	Rassadin, Valentin A
dc.contributor.author	Scholz, Mirko
dc.contributor.author	Klochkova, Anastasiia A
dc.contributor.author	de Meijere, Armin
dc.contributor.author	Sokolov, Victor V
dc.date.accessioned	2019-12-17T13:18:30Z
dc.date.available	2019-12-17T13:18:30Z
dc.date.issued	2017	de
dc.relation.ISSN	1860-5397	de
dc.identifier.uri	http://resolver.sub.uni-goettingen.de/purl?gs-1/17019
dc.description.abstract	A 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.iso	eng	de
dc.rights	openAccess
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/
dc.subject	arylation; fused-ring systems; indole formation; palladium catalysis; sultams	de
dc.subject.ddc	540
dc.title	Synthesis of benzannelated sultams by intramolecular Pd-catalyzed arylation of tertiary sulfonamides	de
dc.type	journalArticle	de
dc.identifier.doi	10.3762/bjoc.13.187
dc.type.version	publishedVersion	de
dc.relation.eISSN	1860-5397
dc.bibliographicCitation.volume	13	de
dc.bibliographicCitation.firstPage	1932	de
dc.bibliographicCitation.lastPage	1939	de
dc.type.subtype	journalArticle
dc.identifier.pmid	29062411
dc.description.status	peerReviewed	de
dc.bibliographicCitation.journal	Beilstein Journal of Organic Chemistry	de

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