C4-Selective C–H Borylation of Pyridinium Derivatives Driven by Electron Donor–Acceptor Complexes

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dc.contributor.authorChoi, Wonjunko
dc.contributor.authorKim, Minseokko
dc.contributor.authorLee, Kangjaeko
dc.contributor.authorPark, Seongjinko
dc.contributor.authorHong, Sungwooko
dc.date.accessioned2023-01-03T05:00:09Z-
dc.date.available2023-01-03T05:00:09Z-
dc.date.created2023-01-03-
dc.date.created2023-01-03-
dc.date.created2023-01-03-
dc.date.issued2022-12-
dc.identifier.citationORGANIC LETTERS, v.24, no.51, pp.9452 - 9457-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10203/303903-
dc.description.abstractThe photoinduced C4-selective C-H borylation of pyridines was achieved using electron donor-acceptor complexes derived from a Lewis base and N-amidopyridinium salts under external oxidant- and photocatalyst-free conditions. Notably, the nucleophilic character of phosphite-ligated boryl radicals enables addition of a radical to position C4 of pyridinium salts to afford C4-borylated heteroarenes that are otherwise difficult to obtain. This approach provides a versatile platform for the installation of both phosphite- and amine-coordinated boron groups on a series of pyridines under mild conditions, demonstrating excellent C4-positional selectivity for the pyridine scaffolds.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleC4-Selective C–H Borylation of Pyridinium Derivatives Driven by Electron Donor–Acceptor Complexes-
dc.typeArticle-
dc.identifier.wosid000901584800001-
dc.identifier.scopusid2-s2.0-85144426594-
dc.type.rimsART-
dc.citation.volume24-
dc.citation.issue51-
dc.citation.beginningpage9452-
dc.citation.endingpage9457-
dc.citation.publicationnameORGANIC LETTERS-
dc.identifier.doi10.1021/acs.orglett.2c03882-
dc.contributor.localauthorHong, Sungwoo-
dc.contributor.nonIdAuthorChoi, Wonjun-
dc.contributor.nonIdAuthorKim, Minseok-
dc.contributor.nonIdAuthorLee, Kangjae-
dc.contributor.nonIdAuthorPark, Seongjin-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusLIGHT-
dc.subject.keywordPlusRADICALS-
dc.subject.keywordPlusSCOPE-
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