Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9708
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dc.contributor.authorPatel, Monaken_US
dc.contributor.authorPANDAY, RISHUKUMARen_US
dc.contributor.authorDholakiya, Bharatkumar Z.en_US
dc.contributor.authorNaveen, Togatien_US
dc.date.accessioned2025-04-22T09:46:10Z-
dc.date.available2025-04-22T09:46:10Z-
dc.date.issued2025-02en_US
dc.identifier.citationOrganic Chemistry Frontiers, 12(03), 754-759.en_US
dc.identifier.issn2052-4129en_US
dc.identifier.urihttps://doi.org/10.1039/D4QO01962Hen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9708-
dc.description.abstractThe chalcogen–nitrogen bond (X–N, where X = S, Se) is a key chemical motif in many structures, including inorganic and organic materials, catalysts, protein mimics, and pharmaceuticals. Consequently, developing mild and general methods for constructing N–S and N–Se bonds is important in organic synthesis. Herein, we have developed a novel copper-catalyzed approach to form N–S/N–Se bonds by coupling amines with 1,2-diphenyl disulfide or diphenyl diselenide. The disclosed platforms demonstrate excellent substrate scope, delivering the desired products in good to excellent yields, and are readily amenable for scale-up. The configuration of the product was confirmed through single-crystal X-ray diffraction analysis. Hitherto, no prior reports have been found in the literature for forming N–Se bonds making this reaction an important breakthrough in synthetic organic chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2025en_US
dc.titleCopper-catalyzed N–H bond chalcogenation of anilinesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Chemistry Frontiersen_US
dc.publication.originofpublisherForeignen_US
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