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Rhodium-Catalyzed Direct CH Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines : Rhodium-Catalyzed Direct C-H Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines

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dc.contributor.authorRyu, Jaeyune-
dc.contributor.authorShin, Kwangmin-
dc.contributor.authorPark, Sae Hume-
dc.contributor.authorKim, Ji Young-
dc.contributor.authorChang, Sukbok-
dc.date.accessioned2023-05-03T05:47:10Z-
dc.date.available2023-05-03T05:47:10Z-
dc.date.created2023-05-01-
dc.date.created2023-05-01-
dc.date.created2023-05-01-
dc.date.issued2012-09-
dc.identifier.citationAngewandte Chemie International Edition, Vol.51 No.39, pp.9904-9908-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://hdl.handle.net/10371/191825-
dc.description.abstractNo muss, no fuss: A rhodium-catalyzed direct intermolecular C-H amination of benzamides and ketoximes using aryl azides as the amine source has been developed. The reaction exhibits a broad substrate scope with excellent functional-group tolerance, requires no external oxidants, releases N 2 as the only by-product, and produces diarylamines in high yields. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.-
dc.language영어-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleRhodium-Catalyzed Direct CH Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines-
dc.title.alternativeRhodium-Catalyzed Direct C-H Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines-
dc.typeArticle-
dc.identifier.doi10.1002/anie.201205723-
dc.citation.journaltitleAngewandte Chemie International Edition-
dc.identifier.wosid000308886800038-
dc.identifier.scopusid2-s2.0-84866524518-
dc.citation.endpage9908-
dc.citation.number39-
dc.citation.startpage9904-
dc.citation.volume51-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorRyu, Jaeyune-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTRANSITION-METAL-COMPLEXES-
dc.subject.keywordPlusN BOND FORMATION-
dc.subject.keywordPlusROOM-TEMPERATURE-
dc.subject.keywordPlusORGANIC AZIDES-
dc.subject.keywordPlusVINYL AZIDES-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusAMIDATION-
dc.subject.keywordPlusCHLOROAMINES-
dc.subject.keywordPlusAZOLES-
dc.subject.keywordPlusFUNCTIONALIZATIONS-
dc.subject.keywordAuthoramination-
dc.subject.keywordAuthoraryl azides-
dc.subject.keywordAuthorC?H activation-
dc.subject.keywordAuthordiarylamines-
dc.subject.keywordAuthorrhodium-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Catalysis, Nano Materials, Physical E-Chem, 무기화학, 물리전기화학

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