Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9521
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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.accessioned2025-04-15T06:51:47Z-
dc.date.available2025-04-15T06:51:47Z-
dc.date.issued2025-01en_US
dc.identifier.citationOrganic Chemistry Frontiers, 12(03), 754-759.en_US
dc.identifier.urihttps://doi.org/10.1039/d4qo01962hen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9521-
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.subjectPeroxidase Mimeticsen_US
dc.subjectSeleniumen_US
dc.subjectSulfenamidesen_US
dc.subjectInhibitorsen_US
dc.subjectAlkynesen_US
dc.subjectThiolsen_US
dc.subjectAgentsen_US
dc.subjectArylen_US
dc.subject2024en_US
dc.titleCopper-catalyzed N-H bond chalcogenation of anilinesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleOrganic Chemistry Frontiersen_US
dc.publication.originofpublisherForeignen_US
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