Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95053
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorMainland Development Officeen_US
dc.creatorChen, Zen_US
dc.creatorGu, Cen_US
dc.creatorYuen, OYen_US
dc.creatorSo, CMen_US
dc.date.accessioned2022-09-13T03:36:57Z-
dc.date.available2022-09-13T03:36:57Z-
dc.identifier.issn2041-6520en_US
dc.identifier.urihttp://hdl.handle.net/10397/95053-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© 2022 The Author(s). Published by the Royal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe 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.titlePalladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C-Cl siteen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage4762en_US
dc.identifier.epage4769en_US
dc.identifier.volume13en_US
dc.identifier.issue17en_US
dc.identifier.doi10.1039/d1sc06701jen_US
dcterms.abstractThis 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.accessRightsopen accessen_US
dcterms.bibliographicCitationChemical science, 7 May 2022, v. 13, no. 17, p. 4762-4769en_US
dcterms.isPartOfChemical scienceen_US
dcterms.issued2022-05-07-
dc.identifier.scopus2-s2.0-85127596220-
dc.identifier.ros2021004406-
dc.identifier.eissn2041-6539en_US
dc.description.validate202209 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberCDCF_2021-2022-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS71013480-
dc.description.oaCategoryCCen_US
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