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Iron(0)-Catalyzed Transfer Hydrogenative Condensation of Nitroarenes with Alcohols: A Straightforward Approach to Benzoxazoles, Benzothiazoles, and Benzimidazoles

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dc.contributor.authorPutta, Ramachandra Reddy-
dc.contributor.authorChun, Simin-
dc.contributor.authorChoi, Seung Hyun-
dc.contributor.authorLee, Seok Beom-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorHong, Suckchang-
dc.date.accessioned2024-05-14T07:16:52Z-
dc.date.available2024-05-14T07:16:52Z-
dc.date.created2021-02-01-
dc.date.issued2020-12-04-
dc.identifier.citationJournal of Organic Chemistry, Vol.85 No.23, pp.15396-15405-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://hdl.handle.net/10371/202001-
dc.description.abstractThe iron-catalyzed hydrogen transfer strategy has been applied to the redox condensation of o-hydroxynitrobenzene with alcohol, leading to the formation of benzoxazole derivatives. A wide range of 2-substituted benzoxazoles were synthesized in good to excellent yields without the addition of an external redox agent. A series of control experiments provided a plausible mechanism. Furthermore, the reaction system was successfully extended to the synthesis of benzothiazoles and benzimidazoles.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleIron(0)-Catalyzed Transfer Hydrogenative Condensation of Nitroarenes with Alcohols: A Straightforward Approach to Benzoxazoles, Benzothiazoles, and Benzimidazoles-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.0c02191-
dc.citation.journaltitleJournal of Organic Chemistry-
dc.identifier.wosid000598137400050-
dc.identifier.scopusid2-s2.0-85096856627-
dc.citation.endpage15405-
dc.citation.number23-
dc.citation.startpage15396-
dc.citation.volume85-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCATALYZED REDOX CONDENSATION-
dc.subject.keywordPlusAEROBIC OXIDATIVE SYNTHESIS-
dc.subject.keywordPlusALPHA-ALKYLATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusSTRATEGY-
dc.subject.keywordPlusPOTENT-
dc.subject.keywordPlusNITROBENZENES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusKETONES-
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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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