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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19111
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2025-07-30T06:36:38Z-
dc.date.available2025-07-30T06:36:38Z-
dc.date.issued2023-
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2048-8030-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19111-
dc.description.abstractRegioselective C-arylation and C,N-diarylation in 2-aryl-2,3-dihydrophthalazine-1,4-diones has been successfully accomplished with diaryliodonium salts under base-mediated slightly modified Pd-catalyzed conditions. These ligand-driven transformations provided a variety of diversely decorated bi(hetero)aryls in good-to-excellent yields, while N-arylated product could be obtained under similar Pd-catalyzed conditions in the absence of a ligand.en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjectChemistryen_US
dc.subjectArylationen_US
dc.subjectBiarylsen_US
dc.subjectCatalysisen_US
dc.subjectPalladiumen_US
dc.subjectTransition metalsen_US
dc.titlePalladium-catalyzed regioselective C-arylation and C, N-diarylation of N-Aryl-2, 3-dihydrophthalazine-1, 4-diones using diaryliodonium saltsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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