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Photocatalytic para-Selective C-H Functionalization of Anilines with Diazomalonates

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dc.contributor.authorKarmakar, Ujjwal-
dc.contributor.authorHwang, Ho Seong-
dc.contributor.authorLee, Yunjeong-
dc.contributor.authorCho, Eun Jin-
dc.date.accessioned2022-10-27T06:40:15Z-
dc.date.available2022-10-27T06:40:15Z-
dc.date.issued2022-08-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/58909-
dc.description.abstractVisible-light-induced para-selective C-H functionalization of anilines over N-H insertion was developed using diazomalonates with the help of an Ir(III) photocatalyst. The para-selective radical-radical cross coupling proceeded via C-centered radical intermediates generated from both anilines and diazomalonates. The photochemistry of anilines could be extended to other N-heterocycles, such as indole and carbazole. The reaction pathway for the selective C-C coupling was validated by electrochemical and photophysical experiments as well as computational studies. © 2022 American Chemical Society.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titlePhotocatalytic para-Selective C-H Functionalization of Anilines with Diazomalonates-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.2c02228-
dc.identifier.bibliographicCitationOrganic Letters, v.24, no.33, pp 6137 - 6141-
dc.description.isOpenAccessN-
dc.identifier.wosid000860016100001-
dc.identifier.scopusid2-s2.0-85136717581-
dc.citation.endPage6141-
dc.citation.number33-
dc.citation.startPage6137-
dc.citation.titleOrganic Letters-
dc.citation.volume24-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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