Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101596
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorJin, Wen_US
dc.creatorZheng, Pen_US
dc.creatorWong, WTen_US
dc.creatorLaw, GLen_US
dc.date.accessioned2023-09-18T07:31:24Z-
dc.date.available2023-09-18T07:31:24Z-
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://hdl.handle.net/10397/101596-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.rightsThis is the peer reviewed version of the following article: W. Jin, P. Zheng, W.-T. Wong, G.-L. Law, Efficient Selenium-Catalyzed Selective C(sp3)−H Oxidation of Benzylpyridines with Molecular Oxygen. Adv. Synth. Catal. 2017, 359, 1588-1593, which has been published in final form at https://doi.org/10.1002/adsc.201601065. 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.subjectC−H oxidationen_US
dc.subjectHeterocyclesen_US
dc.subjectMolecular oxygenen_US
dc.subjectSelenium catalysisen_US
dc.titleEfficient selenium-catalyzed selective C(sp3)−H oxidation of benzylpyridines with molecular oxygenen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1588en_US
dc.identifier.epage1593en_US
dc.identifier.volume359en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1002/adsc.201601065en_US
dcterms.abstractAn efficient selenium-catalyzed direct oxidation of benzylpyridines in aqueous DMSO has been successfully developed by using molecular oxygen as the oxidant. A variety of benzoylpyridines with broad functional group tolerance were obtained in modest to excellent yields and with exclusive chemoselectivity.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced synthesis & catalysis, 2 May 2017, v. 359, no. 9, p. 1588-1593en_US
dcterms.isPartOfAdvanced synthesis & catalysisen_US
dcterms.issued2017-05-02-
dc.identifier.scopus2-s2.0-85011982134-
dc.identifier.eissn1615-4169en_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0691-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6721295-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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