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

Iridium-Catalyzed Direct C-H Amidation with Weakly Coordinating Carbonyl Directing Groups under Mild Conditions

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dc.contributor.authorKim, Jinwooko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2014-09-04T08:36:51Z-
dc.date.available2014-09-04T08:36:51Z-
dc.date.created2014-03-17-
dc.date.created2014-03-17-
dc.date.issued2014-02-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.53, no.8, pp.2203 - 2207-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/190083-
dc.description.abstractAn iridium-catalyzed direct CH amidation of weakly coordinating substrates, in particular of those bearing ester and ketone groups, under very mild conditions has been developed. The observed high reaction efficiency was achieved by the combined use of acetic acid and lithium carbonate as additives.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectBOND ACTIVATION-
dc.subjectAROMATIC ESTERS-
dc.subjectMETAL-COMPLEXES-
dc.subjectARYL AZIDES-
dc.subjectARENES-
dc.subjectAMINATION-
dc.subjectEFFICIENT-
dc.subjectINHIBITORS-
dc.subjectRH-
dc.subjectOLEFINATION-
dc.titleIridium-Catalyzed Direct C-H Amidation with Weakly Coordinating Carbonyl Directing Groups under Mild Conditions-
dc.typeArticle-
dc.identifier.wosid000330908600031-
dc.identifier.scopusid2-s2.0-84893857090-
dc.type.rimsART-
dc.citation.volume53-
dc.citation.issue8-
dc.citation.beginningpage2203-
dc.citation.endingpage2207-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.201310544-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChang, Sukbok-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorazides-
dc.subject.keywordAuthorC-H amidation-
dc.subject.keywordAuthoresters-
dc.subject.keywordAuthoriridium-
dc.subject.keywordAuthorweakly coordinating groups-
dc.subject.keywordPlusBOND ACTIVATION-
dc.subject.keywordPlusAROMATIC ESTERS-
dc.subject.keywordPlusMETAL-COMPLEXES-
dc.subject.keywordPlusARYL AZIDES-
dc.subject.keywordPlusARENES-
dc.subject.keywordPlusAMINATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusRH-
dc.subject.keywordPlusOLEFINATION-
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