Ligand-controlled, Pd/CuH-catalyzed reductive cross-coupling of terminal alkenes and N-heteroaryl bromides

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dc.contributor.authorSeo, Sanghyupko
dc.contributor.authorKim, Donghyeonko
dc.contributor.authorKim, Hyunwooko
dc.date.accessioned2021-10-31T06:42:21Z-
dc.date.available2021-10-31T06:42:21Z-
dc.date.created2021-10-31-
dc.date.created2021-10-31-
dc.date.created2021-10-31-
dc.date.created2021-10-31-
dc.date.created2021-10-31-
dc.date.issued2021-10-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.57, no.85, pp.11240 - 11243-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/288469-
dc.description.abstractThe reductive cross-coupling of terminal alkenes and N-heterocyclic bromides has been demonstrated by ligand optimization of Pd and CuH catalysis. The optimized ligands are Briphos, a pi-acceptor monodentate phosphorus ligand, for Pd catalysis and DTB-DPPBz, a sterically bulky bidentate phosphorus ligand, for CuH catalysis. These conditions were further applied to the gram-scale production of clathryimine B.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleLigand-controlled, Pd/CuH-catalyzed reductive cross-coupling of terminal alkenes and N-heteroaryl bromides-
dc.typeArticle-
dc.identifier.wosid000705632300001-
dc.identifier.scopusid2-s2.0-85118469425-
dc.type.rimsART-
dc.citation.volume57-
dc.citation.issue85-
dc.citation.beginningpage11240-
dc.citation.endingpage11243-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/d1cc04833c-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, Hyunwoo-
dc.contributor.nonIdAuthorKim, Donghyeon-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusNITROGEN-HETEROCYCLES-
dc.subject.keywordPlusPALLADIUM-
dc.subject.keywordPlusTRANSMETALATION-
dc.subject.keywordPlusESTERS-
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