Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100082
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorMainland Development Officeen_US
dc.creatorChen, Zen_US
dc.creatorSo, CMen_US
dc.date.accessioned2023-08-08T01:51:59Z-
dc.date.available2023-08-08T01:51:59Z-
dc.identifier.issn2193-5807en_US
dc.identifier.urihttp://hdl.handle.net/10397/100082-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2021 Wiley-VCH GmbHen_US
dc.rightsThis is the peer reviewed version of the following article: Chen, Z., & So, C. M. (2021). Palladium‐Phenylpyrazolylphosphine‐Catalyzed Cross‐Coupling of Alkenyl Pivalates. Asian Journal of Organic Chemistry, 10(4), 776-779, which has been published in final form at https://doi.org/10.1002/ajoc.202100031. 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.subjectAlkeneen_US
dc.subjectAlkenyl pivalateen_US
dc.subjectCross-couplingen_US
dc.subjectHeterocyclic phosphineen_US
dc.subjectPalladium-catalyzeden_US
dc.titlePalladium-phenylpyrazolylphosphine-catalyzed cross-coupling of alkenyl pivalatesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage776en_US
dc.identifier.epage779en_US
dc.identifier.volume10en_US
dc.identifier.issue4en_US
dc.identifier.doi10.1002/ajoc.202100031en_US
dcterms.abstractPalladium-catalyzed cross-coupling reactions are indispensable tools for C−C bond formation, and new catalyst development remains a powerful driving force in this field. In this study, a new type of easily accessible phenylpyrazole phosphine ligand is developed. The catalyst generated from Pd(OAc)2 and PP-Phos (L15) is highly effective in the palladium-catalyzed cross-coupling of alkenyl pivalates with organomagnesium reagents. The reaction accommodates a broad scope of alkenyl carboxylates under mild conditions, providing an alternative but practical way to the synthesis of multi-substituted alkenes in value.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAsian journal of organic chemistry, Apr. 2021, v. 10, no. 4, p. 776-779en_US
dcterms.isPartOfAsian journal of organic chemistryen_US
dcterms.issued2021-04-
dc.identifier.scopus2-s2.0-85102510240-
dc.identifier.eissn2193-5815en_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0130-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Science, Technology and Innovation Commission of Shenzhen Municipalityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS50657896-
dc.description.oaCategoryGreen (AAM)en_US
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