Cobalt(III)-Catalyzed C-H Amidation of Arenes using Acetoxycarbamates as Convenient Amino Sources under Mild Conditions

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dc.contributor.authorPatel, Pitambarko
dc.contributor.authorChang, Suk-Bokko
dc.date.accessioned2015-04-08T06:41:17Z-
dc.date.available2015-04-08T06:41:17Z-
dc.date.created2015-03-19-
dc.date.created2015-03-19-
dc.date.issued2015-02-
dc.identifier.citationACS CATALYSIS, v.5, no.2, pp.853 - 858-
dc.identifier.issn2155-5435-
dc.identifier.urihttp://hdl.handle.net/10203/195825-
dc.description.abstractThe Co(III)-catalyzed direct C-H amidation of arenes has been developed using O-acylcarbamates as a convenient amino source. This reaction proceeded in high efficiency under external oxidant-free conditions with a broad range of arene substrates, including 6-arylpurines bearing sensitive functional groups, thus furnishing synthetically versatile arene N-carbamate products.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectN BOND FORMATION-
dc.subjectROOM-TEMPERATURE-
dc.subject6-ARYLPURINE NUCLEOSIDES-
dc.subjectPROTECTED ARYLAMINES-
dc.subjectCYTOSTATIC ACTIVITY-
dc.subjectDIRECT AMINATION-
dc.subjectSULFONYL AZIDES-
dc.subjectARYL AZIDES-
dc.subjectACTIVATION-
dc.subjectFUNCTIONALIZATION-
dc.titleCobalt(III)-Catalyzed C-H Amidation of Arenes using Acetoxycarbamates as Convenient Amino Sources under Mild Conditions-
dc.typeArticle-
dc.identifier.wosid000349275300041-
dc.identifier.scopusid2-s2.0-84922730528-
dc.type.rimsART-
dc.citation.volume5-
dc.citation.issue2-
dc.citation.beginningpage853-
dc.citation.endingpage858-
dc.citation.publicationnameACS CATALYSIS-
dc.identifier.doi10.1021/cs501860b-
dc.contributor.localauthorChang, Suk-Bok-
dc.contributor.nonIdAuthorPatel, Pitambar-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcobalt catalysis-
dc.subject.keywordAuthorC-H amidation-
dc.subject.keywordAuthoracetoxycarbamates-
dc.subject.keywordAuthor6-arylpurines-
dc.subject.keywordAuthorarylamines-
dc.subject.keywordPlusN BOND FORMATION-
dc.subject.keywordPlusROOM-TEMPERATURE-
dc.subject.keywordPlus6-ARYLPURINE NUCLEOSIDES-
dc.subject.keywordPlusPROTECTED ARYLAMINES-
dc.subject.keywordPlusCYTOSTATIC ACTIVITY-
dc.subject.keywordPlusDIRECT AMINATION-
dc.subject.keywordPlusSULFONYL AZIDES-
dc.subject.keywordPlusARYL AZIDES-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusFUNCTIONALIZATION-
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