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One-Pot Synthesis of 4-Quinolone via Iron-Catalyzed Oxidative Coupling of Alcohol and Methyl Arene

DC Field Value Language
dc.contributor.authorLee, Seok Beom-
dc.contributor.authorJang, Yoonkyung-
dc.contributor.authorAhn, Jiwon-
dc.contributor.authorChun, Simin-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorHong, Suckchang-
dc.date.accessioned2024-05-14T07:16:59Z-
dc.date.available2024-05-14T07:16:59Z-
dc.date.created2021-02-01-
dc.date.issued2020-11-06-
dc.identifier.citationOrganic Letters, Vol.22 No.21, pp.8382-8386-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://hdl.handle.net/10371/202003-
dc.description.abstractHerein, we describe the iron(III)-catalyzed oxidative coupling of alcohol/methyl arene with 2-amino phenyl ketone to synthesize 4-quinolone. Alcohols and methyl arenes are oxidized to the aldehyde in the presence of an iron catalyst and di-tert-butyl peroxide, followed by a tandem process, condensation with amine/Mannich-type cyclization/oxidation, to complete the 4-quinolone ring. This method tolerates various kinds of functional groups and provides a direct approach to the synthesis of 4-quinolones from less functionalized substrates.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleOne-Pot Synthesis of 4-Quinolone via Iron-Catalyzed Oxidative Coupling of Alcohol and Methyl Arene-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.0c03011-
dc.citation.journaltitleOrganic Letters-
dc.identifier.wosid000589942900038-
dc.identifier.scopusid2-s2.0-85095861249-
dc.citation.endpage8386-
dc.citation.number21-
dc.citation.startpage8382-
dc.citation.volume22-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusANTITUMOR AGENTS-
dc.subject.keywordPlus2-ARYL-4-QUINOLONES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusAMIDATION-
dc.subject.keywordPlusSCAFFOLD-
dc.subject.keywordPlusARYL-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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