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 |