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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

Iridium-Catalyzed Direct Arene C-H Bond Amidation with Sulfonyl- and Aryl Azides

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dc.contributor.authorLee, Donggunko
dc.contributor.authorKim, Youngchanko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2014-08-28T08:18:25Z-
dc.date.available2014-08-28T08:18:25Z-
dc.date.created2013-12-12-
dc.date.created2013-12-12-
dc.date.issued2013-11-
dc.identifier.citationJOURNAL OF ORGANIC CHEMISTRY, v.78, no.21, pp.11102 - 11109-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/10203/188471-
dc.description.abstractIridium-catalyzed direct ortho C-H amidation of arenes has been shown to work well with sulfonyl- and aryl azides as the nitrogen source. The reaction proceeds efficiently with a broad range of substrates bearing conventional directing groups with excellent functional group compatibility under mild conditions. In addition, substrates forming not only 5- but also 6-membered iridacycle intermediates undergo the C-H amidation with high selectivity.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCARBON-NITROGEN BONDS-
dc.subjectMETAL-FREE CONDITIONS-
dc.subjectDIRECT AMINATION-
dc.subjectCOUPLING REACTIONS-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectBETA-DIKETIMINES-
dc.subjectROOM-TEMPERATURE-
dc.subjectN-CHLOROAMINES-
dc.subjectCOMPLEXES-
dc.subjectFUNCTIONALIZATION-
dc.titleIridium-Catalyzed Direct Arene C-H Bond Amidation with Sulfonyl- and Aryl Azides-
dc.typeArticle-
dc.identifier.wosid000326615300059-
dc.identifier.scopusid2-s2.0-84887036529-
dc.type.rimsART-
dc.citation.volume78-
dc.citation.issue21-
dc.citation.beginningpage11102-
dc.citation.endingpage11109-
dc.citation.publicationnameJOURNAL OF ORGANIC CHEMISTRY-
dc.identifier.doi10.1021/jo4019683-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.nonIdAuthorLee, Donggun-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCARBON-NITROGEN BONDS-
dc.subject.keywordPlusMETAL-FREE CONDITIONS-
dc.subject.keywordPlusDIRECT AMINATION-
dc.subject.keywordPlusCOUPLING REACTIONS-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusBETA-DIKETIMINES-
dc.subject.keywordPlusROOM-TEMPERATURE-
dc.subject.keywordPlusN-CHLOROAMINES-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusFUNCTIONALIZATION-
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