Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101526
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorMainland Development Office-
dc.creatorChen, Xen_US
dc.creatorChen, Zen_US
dc.creatorSo, CMen_US
dc.date.accessioned2023-09-18T07:30:43Z-
dc.date.available2023-09-18T07:30:43Z-
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://hdl.handle.net/10397/101526-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2019 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.joc.9b00669.en_US
dc.titleExploration of aryl phosphates in palladium-catalyzed mono-α-arylation of aryl and heteroaryl ketonesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage6337en_US
dc.identifier.epage6346en_US
dc.identifier.volume84en_US
dc.identifier.issue10en_US
dc.identifier.doi10.1021/acs.joc.9b00669en_US
dcterms.abstractThis paper presents the first general examples of selective palladium-catalyzed mono-α-arylation of aryl and heteroaryl ketones with aryl phosphates. The catalyst system, consisting of [Pd(2-butenyl)Cl]2 and MorDalPhos, exhibited high catalytic reactivity toward this reaction. A wide range of aryl phosphates were efficiently coupled with aryl and heteroaryl ketones with good selectivity. Excellent-to-good product yields were afforded. The gram-scale reaction was conducted smoothly. Reductive elimination or transmetalation might be a rate-determining step in this reaction.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of organic chemistry, 17 May 2019, v. 84, no. 10, p. 6337-6346en_US
dcterms.isPartOfJournal of organic chemistryen_US
dcterms.issued2019-05-17-
dc.identifier.scopus2-s2.0-85065795612-
dc.identifier.pmid31045364-
dc.identifier.eissn1520-6904en_US
dc.description.validate202308 bckw-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0393-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe Hong Kong Polytechnic University Start-up Fund; Shenzhen Strategic New Industry Development Research Fund of Shenzhen Science, Technology and Innovation Commissionen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS13911022-
dc.description.oaCategoryGreen (AAM)en_US
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