Reductive Activation of Pd-II-Precatalysts via Decarboxylation of Pivalate in Direct C-H Arylation Reactions

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dc.contributor.authorKim, Seoung-Taeko
dc.contributor.authorBaik, Mu-Hyunko
dc.date.accessioned2020-12-23T05:50:04Z-
dc.date.available2020-12-23T05:50:04Z-
dc.date.created2020-12-22-
dc.date.created2020-12-22-
dc.date.created2020-12-22-
dc.date.issued2020-11-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.56, no.89, pp.13868 - 13871-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/278942-
dc.description.abstractThe mechanism of the reductive activation of Pd-II pre-catalysts has been extensively studied, but remains poorly understood. Herein, a combined computational and experimental approach is employed to clearly identify a Pd-II reduction process that has not been considered thus far. Pivalate, assumed to be a general base, was found to decarboxylate and act as a reductant, suggesting an alternative explanation for the superior performance of pivalic acid as an additive in Pd-catalyzed direct C-H arylation reactions.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleReductive Activation of Pd-II-Precatalysts via Decarboxylation of Pivalate in Direct C-H Arylation Reactions-
dc.typeArticle-
dc.identifier.wosid000588197200032-
dc.identifier.scopusid2-s2.0-85096061895-
dc.type.rimsART-
dc.citation.volume56-
dc.citation.issue89-
dc.citation.beginningpage13868-
dc.citation.endingpage13871-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/d0cc06085b-
dc.contributor.localauthorBaik, Mu-Hyun-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCATALYZED COUPLING REACTIONS-
dc.subject.keywordPlusZEROVALENT PALLADIUM-
dc.subject.keywordPlusARYL HALIDES-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusDEHALOGENATION-
dc.subject.keywordPlusPD(OAC)(2)-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusMIXTURES-
dc.subject.keywordPlusRATES-
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CH-Journal Papers(저널논문)
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