Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118486
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorPeng, Z-
dc.creatorGu, C-
dc.creatorYuen, OY-
dc.creatorNg, SS-
dc.creatorSo, CM-
dc.date.accessioned2026-04-17T08:27:40Z-
dc.date.available2026-04-17T08:27:40Z-
dc.identifier.issn1861-4728-
dc.identifier.urihttp://hdl.handle.net/10397/118486-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.subjectChemoselectivityen_US
dc.subjectChloroaryl triflatesen_US
dc.subjectDirect arylationen_US
dc.subjectPhosphine liganden_US
dc.subjectPolyfluoroareneen_US
dc.titlePalladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloroaryl triflates at the C–Cl bonden_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume20-
dc.identifier.issue24-
dc.identifier.doi10.1002/asia.202500949-
dcterms.abstractThis study describes a palladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloro(hetero)aryl triflates, achieving site-selective functionalization at the C–Cl bond for the first time. The recently developed alkyl-pyrazole-based phosphine ligand (BirdPhos) proved essential for the success of this transformation, affording excellent yields with high chemoselectivity. Moreover, the catalytic system enables the efficient synthesis of a broad range of functionalized polyfluoroarene derivatives under mild, additive-free conditions. Notably, the reaction retains the triflate group in the products, providing a versatile functional handle for further derivatization and highlighting the broad applicability and synthetic utility of this method.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationChemistry, an Asian journal, 15 Dec. 2025, v. 20, no. 24, e00949-
dcterms.isPartOfChemistry, an Asian journal-
dcterms.issued2025-12-15-
dc.identifier.scopus2-s2.0-105021947284-
dc.identifier.pmid41236121-
dc.identifier.eissn1861-471X-
dc.identifier.artne00949-
dc.description.validate202604 bcjz-
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001455/2026-01en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingTextThe authors thank the Research Grants Council of the Hong Kong Special Administrative Region, China (PolyU 15304124 and 15305522) for financial support.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-12-15en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2026-12-15
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