Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95269
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorFu, WCen_US
dc.creatorZhou, Zen_US
dc.creatorKwong, FYen_US
dc.date.accessioned2022-09-14T08:32:55Z-
dc.date.available2022-09-14T08:32:55Z-
dc.identifier.issn2052-4129en_US
dc.identifier.urihttp://hdl.handle.net/10397/95269-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © the Partner Organisations 2016en_US
dc.rightsThe following publication Fu, W. C., Zhou, Z., & Kwong, F. Y. (2016). A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses. Organic Chemistry Frontiers, 3(2), 273–276 is available at https://doi.org/10.1039/C5QO00400D.en_US
dc.titleA benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl synthesesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage273en_US
dc.identifier.epage276en_US
dc.identifier.volume3en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1039/c5qo00400den_US
dcterms.abstractA new benzo[c]carbazolyl-based phosphine ligand has been designed and synthesized. This newly developed ligand efficiently facilitates the Pd-catalyzed tetra-ortho-substituted biaryl syntheses via Suzuki-Miyaura cross-coupling. With 1 mol% of the Pd(OAc)2/L6 catalyst, sterically congested biaryls were afforded in good-to-excellent yields. In particular, the mild reaction conditions exhibited good compatibility of heterocycles and functional groups including esters and nitrile. L6 was structurally characterized by X-ray crystallographic analysis.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic chemistry frontiers, 1 Feb. 2016, v. 3, no. 2, p. 273-276en_US
dcterms.isPartOfOrganic chemistry frontiersen_US
dcterms.issued2016-02-01-
dc.identifier.scopus2-s2.0-85000786958-
dc.description.validate202209 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberRGC-B2-1521, ABCT-0793en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextState Key Laboratory of Chirosciencesen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS54688614en_US
dc.description.oaCategoryGreen (AAM)en_US
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