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N-Arylation of Sterically Hindered NH-Nucleophiles: Copper-Mediated Syntheses of Diverse N-Arylindole-2-carboxylates

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dc.contributor.authorLee, Jinyong-
dc.contributor.authorChoi, Ji Hye-
dc.contributor.authorShin, Seunghoon-
dc.contributor.authorHeo, Jung-Nyoung-
dc.contributor.authorLim, Hwan Jung-
dc.date.accessioned2022-07-07T03:57:56Z-
dc.date.available2022-07-07T03:57:56Z-
dc.date.created2021-05-12-
dc.date.issued2015-11-
dc.identifier.issn0039-7881-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/142884-
dc.description.abstractIndole-carboxylates are N-arylated with 2-bromopyridines using stoichiometric copper(II) oxide/potassium carbonate to give various N-(2-pyridyl)-substituted indole-2-carboxylates and with bromobenzenes using stoichiometric copper(I) iodide/N,N'-dimethylethylenediamine to give various N-(substituted phenyl)-substituted indole-2-carboxylates. These results expand the scope of metal-catalyzed N-arylation using heterocyclic amines with steric bulk and weak nucleophilicity.-
dc.language영어-
dc.language.isoen-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleN-Arylation of Sterically Hindered NH-Nucleophiles: Copper-Mediated Syntheses of Diverse N-Arylindole-2-carboxylates-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Seunghoon-
dc.identifier.doi10.1055/s-0035-1560065-
dc.identifier.wosid000364224700009-
dc.identifier.bibliographicCitationSYNTHESIS-STUTTGART, v.47, no.21, pp.3301 - 3308-
dc.relation.isPartOfSYNTHESIS-STUTTGART-
dc.citation.titleSYNTHESIS-STUTTGART-
dc.citation.volume47-
dc.citation.number21-
dc.citation.startPage3301-
dc.citation.endPage3308-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusNITROGEN-CONTAINING HETEROCYCLES-
dc.subject.keywordPlusC-N-
dc.subject.keywordPlusFISCHER INDOLIZATION-
dc.subject.keywordPlusARYL HALIDES-
dc.subject.keywordPlusINDOLES-
dc.subject.keywordPlusPALLADIUM-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusULLMANN-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordAuthorcopper-
dc.subject.keywordAuthorN-arylation-
dc.subject.keywordAuthorindoles-
dc.subject.keywordAuthorcopper-mediated synthesis-
dc.subject.keywordAuthorheterocyclic amines-
dc.subject.keywordAuthormetal-catalyzed-
dc.identifier.urlhttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0035-1560065-
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