Synthesis of Redox-Active Phenanthrene-Fused Heteroarenes by Palladium-Catalyzed C-H Annulation

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dc.contributor.authorJang, Jin Hyeokko
dc.contributor.authorAhn, Seongmoko
dc.contributor.authorPark, Soo Eunko
dc.contributor.authorKim, Soeunko
dc.contributor.authorByon, Hye Ryungko
dc.contributor.authorJoo, Jung Minko
dc.date.accessioned2020-10-21T02:55:30Z-
dc.date.available2020-10-21T02:55:30Z-
dc.date.created2020-04-14-
dc.date.issued2020-02-
dc.identifier.citationORGANIC LETTERS, v.22, no.4, pp.1280 - 1285-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10203/276772-
dc.description.abstractPd-catalyzed C-H annulation reactions of halo- and aryl-heteroarenes were developed using readily available o-bromobiaryls and o-dibromoaryls, respectively. A variety of five-membered heteroarenes rapidly provided the corresponding phenanthrene-fused heteroarenes, which led to the identification of phenanthro-pyrazole and thiazole as new, stable -2 V redox couples. The flexible syntheses and tunability of the redox potentials of these azole-fused phenanthrenes over a wide range are expected to facilitate their application as redox-active organic functional materials.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleSynthesis of Redox-Active Phenanthrene-Fused Heteroarenes by Palladium-Catalyzed C-H Annulation-
dc.typeArticle-
dc.identifier.wosid000516667200012-
dc.identifier.scopusid2-s2.0-85079802503-
dc.type.rimsART-
dc.citation.volume22-
dc.citation.issue4-
dc.citation.beginningpage1280-
dc.citation.endingpage1285-
dc.citation.publicationnameORGANIC LETTERS-
dc.identifier.doi10.1021/acs.orglett.9b04545-
dc.contributor.localauthorByon, Hye Ryung-
dc.contributor.nonIdAuthorJang, Jin Hyeok-
dc.contributor.nonIdAuthorPark, Soo Eun-
dc.contributor.nonIdAuthorJoo, Jung Min-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFLOW BATTERIES-
dc.subject.keywordPlusPI-EXTENSION-
dc.subject.keywordPlusDIRECT ARYLATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMEDIATORS-
dc.subject.keywordPlusPYRAZOLES-
dc.subject.keywordPlusINDOLES-
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