Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/110510
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorMainland Development Office-
dc.creatorGu, Cen_US
dc.creatorSo, CMen_US
dc.date.accessioned2024-12-17T00:43:21Z-
dc.date.available2024-12-17T00:43:21Z-
dc.identifier.urihttp://hdl.handle.net/10397/110510-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2024 The Authors. Advanced Science published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication C. Gu, C. M. So, Regio- and Chemoselective Palladium-Catalyzed Additive-Free Direct C─H Functionalization of Heterocycles with Chloroaryl Triflates Using Pyrazole-Alkyl Phosphine Ligands. Adv. Sci. 2024, 11, 2309192 is available at https://doi.org/10.1002/advs.202309192.en_US
dc.subjectChemoselectivityen_US
dc.subjectC─H arylationen_US
dc.subjectPalladiumen_US
dc.subjectPhosphineen_US
dc.subjectRegioselectivityen_US
dc.titleRegio- and chemoselective palladium-catalyzed additive-free direct C─H functionalization of heterocycles with chloroaryl triflates using pyrazole-alkyl phosphine ligandsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume11en_US
dc.identifier.issue21en_US
dc.identifier.doi10.1002/advs.202309192en_US
dcterms.abstractA series of new pyrazole-alkyl phosphine ligands with varying cycloalkyl ring sizes that enable additive-free regio- and chemoselective C─H arylation of heterocycles are reported. Excellent α/β selectivity of various heterocycles such as benzo[b]thiophene, thiophene, furan, benzofuran, and thiazole can be achieved using these ligands, along with excellent chemoselectivity of C─Cl over C─OTf of chloroaryl triflates. Mechanistic studies supported by both experimental findings and density functional theory calculations indicate that the pyrazole phosphine ligands with optimal ring sizes allow the reaction to proceed with a lower energy barrier via a concerted metalation–deprotonation pathway.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 5 June 2024, v. 11, no. 21, 2309192en_US
dcterms.isPartOfAdvanced scienceen_US
dcterms.issued2024-06-05-
dc.identifier.scopus2-s2.0-85187692828-
dc.identifier.eissn2198-3844en_US
dc.identifier.artn2309192en_US
dc.description.validate202412 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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