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유전체항상성연구단
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An Annulative Synthetic Strategy for Building Triphenylene Frameworks by Multiple C−H Bond Activations

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dc.contributor.authorBijoy P. Mathew-
dc.contributor.authorHyun Ji Yang-
dc.contributor.authorJoohee Kim-
dc.contributor.authorJae Bin Lee-
dc.contributor.authorYun-Tae Kim-
dc.contributor.authorSungmin Lee-
dc.contributor.authorChang Young Lee-
dc.contributor.authorWonyoung Choe-
dc.contributor.authorKyungjae Myung-
dc.contributor.authorJang-Ung Park-
dc.contributor.authorSung You Hong-
dc.date.available2018-01-08T05:16:54Z-
dc.date.created2017-05-19-
dc.date.issued2017-04-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4180-
dc.description.abstractC−H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy demands on multiple catalytic cycle operations and site-selectivity have limited its use for graphene segment synthesis. A Pd-catal- yzed one-step synthesis of functionalized triphenylene frameworks is disclosed, which proceeds by 2- or 4-fold C−H arylation of unactivated benzene derivatives. A Pd2(dibenzylideneacetone)3 catalytic system, using cyclic diaryliodonium salts as π-extending agents, leads to site-selective inter- and intramolecular tandem arylation sequences. Moreover, N-substituted triphenylenes are applied to a field-effect transistor sensor for rapid, sensitive, and reversible alcohol vapor detection. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinhei-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectarylation-
dc.subjectC−H activation-
dc.subjectdiaryliodonium salt-
dc.subjectpalladium-
dc.subjecttriphenylene-
dc.titleAn Annulative Synthetic Strategy for Building Triphenylene Frameworks by Multiple C−H Bond Activations-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000399384700018-
dc.identifier.scopusid2-s2.0-85016982079-
dc.identifier.rimsid59480ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorBijoy P. Mathew-
dc.contributor.affiliatedAuthorKyungjae Myung-
dc.contributor.affiliatedAuthorSung You Hong-
dc.identifier.doi10.1002/anie.201700405-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.18, pp.5007 - 5011-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume56-
dc.citation.number18-
dc.citation.startPage5007-
dc.citation.endPage5011-
dc.date.scptcdate2018-10-01-
dc.description.wostc14-
dc.description.scptc13-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusGRAPHENE NANORIBBONS-
dc.subject.keywordPlusCATALYZED ANNULATION-
dc.subject.keywordPlusCARBON NANOTUBES-
dc.subject.keywordPlusPALLADIUM-
dc.subject.keywordPlusNANOGRAPHENE-
dc.subject.keywordPlusNANOSTRUCTURES-
dc.subject.keywordPlusTRANSPARENT-
dc.subject.keywordPlusARYLATION-
dc.subject.keywordPlusUNIFORM-
dc.subject.keywordPlusARYNES-
dc.subject.keywordAuthorarylation-
dc.subject.keywordAuthorC-H activation-
dc.subject.keywordAuthordiaryliodonium salt-
dc.subject.keywordAuthorpalladium-
dc.subject.keywordAuthortriphenylene-
Appears in Collections:
Center for Genomic Integrity(유전체 항상성 연구단) > 1. Journal Papers (저널논문)
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