Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101610
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorMainland Development Officeen_US
dc.creatorYuen, OYen_US
dc.creatorSo, CMen_US
dc.creatorMan, HWen_US
dc.creatorKwong, FYen_US
dc.date.accessioned2023-09-18T07:31:32Z-
dc.date.available2023-09-18T07:31:32Z-
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://hdl.handle.net/10397/101610-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.rightsThis is the peer reviewed version of the following article: O. Y. Yuen, C. M. So, H. W. Man, F. Y. Kwong, A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides. Chem. Eur. J. 2016, 22, 6471-6476, which has been published in final form at https://doi.org/10.1002/chem.201600420. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectAryl chloridesen_US
dc.subjectAryl(alkoxy)silaneen_US
dc.subjectCross-coupling reactionen_US
dc.subjectPalladiumen_US
dc.subjectPhosphine liganden_US
dc.titleA general palladium-catalyzed Hiyama cross-coupling reaction of aryl and heteroaryl chloridesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage6471en_US
dc.identifier.epage6476en_US
dc.identifier.volume22en_US
dc.identifier.issue19en_US
dc.identifier.doi10.1002/chem.201600420en_US
dcterms.abstractA general palladium-catalyzed Hiyama cross-coupling reaction of aryl and heteroaryl chlorides with aryl and heteroaryl trialkoxysilanes by a Pd(OAc)2/L2 catalytic system is presented. A newly developed water addition protocol can dramatically improve the product yields. The conjugation of the Pd/L2 system and the water addition protocol can efficiently catalyze a broad range of electron-rich, -neutral, -deficient, and sterically hindered aryl chlorides and heteroaryl chlorides with excellent yields within three hours and the catalyst loading can be down to 0.05 mol % Pd for the first time. Hiyama coupling of heteroaryl chlorides with heteroaryl silanes is also reported for the first time. The reaction can be easily scaled up 200 times (100 mmol) without any degasification and purification of reactants; this facilitates the practical application in routine synthesis.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChemistry - a European journal, 4 May 2016, v. 22, no. 19, p. 6471-6476en_US
dcterms.isPartOfChemistry - a European journalen_US
dcterms.issued2016-05-04-
dc.identifier.scopus2-s2.0-84978017057-
dc.identifier.eissn1521-3765en_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0764-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6658150-
dc.description.oaCategoryGreen (AAM)en_US
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