Copper-(s)-n-methylpyrrolidine-2-carboxylate Catalyzed N-arylation Of N5h-1,2,5-thiadiazolidine 1,1-dioxides

dc.contributor.authorDehamchia, M.
dc.contributor.authorRegaïnia, Z.
dc.date.accessioned2020-10-22T08:55:49Z
dc.date.available2020-10-22T08:55:49Z
dc.date.issued2016-01-01
dc.descriptionArticale in Journal of fundamental and Applied Sciences Vol. 08, N. 01en_US
dc.description.abstractA copper-catalyzed N-arylation of N5H-1,2,5-thiadiazolidine 1,1-dioxides derivatives (cyclic sulfamides) is described. Reactions were carried out using Ullmann–Goldberg-type condensation with (S)-N-methyl-2-carboxylate as the ligand, and N-arylated products were obtained with moderate to good yields. The structures of the synthesized compounds were confirmed based on analytical and spectral data.en_US
dc.identifier.citationArticale in Journal of fundamental and Applied Sciences Vol. 08, N. 01en_US
dc.identifier.issn1112-9867
dc.identifier.urihttp://dspace.univ-eloued.dz/handle/123456789/7264
dc.language.isoenen_US
dc.publisherUniversity of Eloued جامعة الواديen_US
dc.subjectUllmann reaction; Goldberg reaction; N-arylation; 1, 2, 5-thiadiazolidine 1, 1-dioxides; aryl halide.en_US
dc.titleCopper-(s)-n-methylpyrrolidine-2-carboxylate Catalyzed N-arylation Of N5h-1,2,5-thiadiazolidine 1,1-dioxidesen_US
dc.typeArticleen_US

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