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Mechanism of action of base-catalyzed oxygenation of phenol derivatives

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dc.contributor.authorLee, Duck-Hyung-
dc.contributor.authorSon, Jung Beom-
dc.contributor.authorJung, Seokwon-
dc.contributor.authorSong, Jihey-
dc.contributor.authorHam, Seung Wook-
dc.date.available2019-05-30T07:35:31Z-
dc.date.issued2005-11-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24480-
dc.description.abstractCyclopropyl derivative of 2,6-di-tert-butylphenol is synthesized as a probe to investigate the mechanism of base-catalyzed autooxidation of phenol derivatives. Our study indicates that one electron reduction of molecular oxygen from phenolate gives phenoxyl radical 3, a key intermediate of autooxidation. The coupling of phenoxyl radical and superoxide radical gives peroxylate anion 4 and produces the final epoxy alcohol adduct 6. (c) 2005 Published by Elsevier Ltd.-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleMechanism of action of base-catalyzed oxygenation of phenol derivatives-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2005.09.029-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.46, no.45, pp 7721 - 7723-
dc.description.isOpenAccessN-
dc.identifier.wosid000232738500012-
dc.identifier.scopusid2-s2.0-26444602000-
dc.citation.endPage7723-
dc.citation.number45-
dc.citation.startPage7721-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume46-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordAuthorautooxidation-
dc.subject.keywordAuthorphenolate-
dc.subject.keywordAuthormechanism-
dc.subject.keywordAuthorradical-
dc.subject.keywordPlusPICOSECOND RADICAL KINETICS-
dc.subject.keywordPlusPOTASSIUM SUPEROXIDE-
dc.subject.keywordPlusVITAMIN-K-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusION-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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