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  Department of Chemistry (화학과) 1. Journal Papers

 

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Cited 345 time in webofscience Cited 347 time in scopus
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dc.contributor.authorKim, HJ-
dc.contributor.authorKim, J-
dc.contributor.authorCho, SH-
dc.contributor.authorChang, S-
dc.date.accessioned2016-03-31T08:02:47Z-
dc.date.available2016-03-31T08:02:47Z-
dc.date.created2014-07-31-
dc.date.issued2011-10-19-
dc.identifier.issn0002-7863-
dc.identifier.other2011-OAK-0000030156-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/14437-
dc.description.abstractA new synthetic approach toward intermolecular oxidative C-N bond formation of arenes has been developed under transition-metal-free conditions. Complete control of chemoselectivity between aryl sp(2) and benzylic sp(3) C-H bond imidation was achieved by the choice of nitrogen sources, representatively being phthalimide and dibenzenesulfonimide, respectively.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.subjectELECTROPHILIC AROMATIC-SUBSTITUTION-
dc.subjectHYPERVALENT IODINE COMPOUNDS-
dc.subjectCATALYZED DIRECT AMINATION-
dc.subjectNITRENIUM IONS-
dc.subjectHETEROCYCLIC-COMPOUNDS-
dc.subjectAMBIENT-TEMPERATURE-
dc.subjectACYLNITRENIUM IONS-
dc.subjectSINGLE-ELECTRON-
dc.subjectAMIDATION-
dc.subjectROUTE-
dc.titleIntermolecular oxidative C-N bond formation under metal-free conditions: Control of Chemoselectivity between Aryl sp(2) and Benzylic sp(3) C-H Bond Imidation-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/JA207296Y-
dc.author.googleKim, HJ-
dc.author.googleKim, J-
dc.author.googleCho, SH-
dc.author.googleChang, S-
dc.relation.volume133-
dc.relation.issue41-
dc.relation.startpage16382-
dc.relation.lastpage16385-
dc.contributor.id11362690-
dc.relation.journalJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.133, no.41, pp.16382 - 16385-
dc.identifier.wosid000295997500017-
dc.date.tcdate2019-01-01-
dc.citation.endPage16385-
dc.citation.number41-
dc.citation.startPage16382-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume133-
dc.contributor.affiliatedAuthorCho, SH-
dc.identifier.scopusid2-s2.0-80054764821-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc248-
dc.description.scptc229*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusELECTROPHILIC AROMATIC-SUBSTITUTION-
dc.subject.keywordPlusHYPERVALENT IODINE COMPOUNDS-
dc.subject.keywordPlusCATALYZED DIRECT AMINATION-
dc.subject.keywordPlusACYLNITRENIUM IONS-
dc.subject.keywordPlusSINGLE-ELECTRON-
dc.subject.keywordPlusAMIDATION-
dc.subject.keywordPlusROUTE-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusARENES-
dc.subject.keywordPlusAZOLES-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
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조승환CHO, SEUNG HWAN
Dept of Chemistry
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