Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/95053
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
| dc.contributor | Mainland Development Office | en_US |
| dc.creator | Chen, Z | en_US |
| dc.creator | Gu, C | en_US |
| dc.creator | Yuen, OY | en_US |
| dc.creator | So, CM | en_US |
| dc.date.accessioned | 2022-09-13T03:36:57Z | - |
| dc.date.available | 2022-09-13T03:36:57Z | - |
| dc.identifier.issn | 2041-6520 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/95053 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.rights | © 2022 The Author(s). Published by the Royal Society of Chemistry | en_US |
| dc.rights | This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/). | en_US |
| dc.rights | The following publication Chen, Z., Gu, C., Yuen, O. Y., & So, C. M. (2022). Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site. Chemical Science, 13(17), 4762-4769 is available at https://doi.org/10.1039/D1SC06701J. | en_US |
| dc.title | Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C-Cl site | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 4762 | en_US |
| dc.identifier.epage | 4769 | en_US |
| dc.identifier.volume | 13 | en_US |
| dc.identifier.issue | 17 | en_US |
| dc.identifier.doi | 10.1039/d1sc06701j | en_US |
| dcterms.abstract | This study described palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates in the Ar-Cl bond. The Pd/SelectPhos system showed excellent chemoselectivity toward the Ar-Cl bond in the presence of the Ar-OTf bond with a broad substrate scope and excellent product yields. The electronic and steric hindrance offered by the -PR2 group of the ligand with the C2-alkyl group was found to be the key factor affecting the reactivity and chemoselectivity of the α-arylation reaction. The chemodivergent approach was also successfully employed in the synthesis of flurbiprofen and its derivatives (e.g., -OMe and -F). | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Chemical science, 7 May 2022, v. 13, no. 17, p. 4762-4769 | en_US |
| dcterms.isPartOf | Chemical science | en_US |
| dcterms.issued | 2022-05-07 | - |
| dc.identifier.scopus | 2-s2.0-85127596220 | - |
| dc.identifier.ros | 2021004406 | - |
| dc.identifier.eissn | 2041-6539 | en_US |
| dc.description.validate | 202209 bchy | en_US |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | CDCF_2021-2022 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | National Natural Science Foundation of China | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.identifier.OPUS | 71013480 | - |
| dc.description.oaCategory | CC | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Chen_Palladium-catalyzed_chemoselective_direct.pdf | 2 MB | Adobe PDF | View/Open |
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