Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/118486
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | - |
| dc.creator | Peng, Z | - |
| dc.creator | Gu, C | - |
| dc.creator | Yuen, OY | - |
| dc.creator | Ng, SS | - |
| dc.creator | So, CM | - |
| dc.date.accessioned | 2026-04-17T08:27:40Z | - |
| dc.date.available | 2026-04-17T08:27:40Z | - |
| dc.identifier.issn | 1861-4728 | - |
| dc.identifier.uri | http://hdl.handle.net/10397/118486 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-VCH | en_US |
| dc.subject | Chemoselectivity | en_US |
| dc.subject | Chloroaryl triflates | en_US |
| dc.subject | Direct arylation | en_US |
| dc.subject | Phosphine ligand | en_US |
| dc.subject | Polyfluoroarene | en_US |
| dc.title | Palladium-catalyzed chemoselective direct arylation of polyfluoroarenes with chloroaryl triflates at the C–Cl bond | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 20 | - |
| dc.identifier.issue | 24 | - |
| dc.identifier.doi | 10.1002/asia.202500949 | - |
| dcterms.abstract | This 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.accessRights | embargoed access | en_US |
| dcterms.bibliographicCitation | Chemistry, an Asian journal, 15 Dec. 2025, v. 20, no. 24, e00949 | - |
| dcterms.isPartOf | Chemistry, an Asian journal | - |
| dcterms.issued | 2025-12-15 | - |
| dc.identifier.scopus | 2-s2.0-105021947284 | - |
| dc.identifier.pmid | 41236121 | - |
| dc.identifier.eissn | 1861-471X | - |
| dc.identifier.artn | e00949 | - |
| dc.description.validate | 202604 bcjz | - |
| dc.description.oa | Not applicable | en_US |
| dc.identifier.SubFormID | G001455/2026-01 | en_US |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingText | The 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.pubStatus | Published | en_US |
| dc.date.embargo | 2026-12-15 | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
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