DSpace at KISTKIST Article2001

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dc.contributor.authorKim, EH-
dc.contributor.authorKoo, BS-
dc.contributor.authorSong, CE-
dc.contributor.authorLee, KJ-
dc.date.accessioned2024-01-21T11:39:00Z-
dc.date.available2024-01-21T11:39:00Z-
dc.date.created2021-09-05-
dc.date.issued2001-11-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140089-
dc.description.abstractAromatic methyl ketones undergo alpha -halogenation on treatment with sodium halide in the presence of oxone (R) in aqueous methanol. However, electron-rich hetero aromatic methyl ketones afford ring bromination products preferentially.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectOXIDATIVE CLEAVAGE-
dc.subjectPEPTIDE-SYNTHESIS-
dc.subjectDIOXIRANE-
dc.subjectCARBONYL-
dc.titleHalogenation of aromatic methyl ketones using Oxone (R) and sodium halide-
dc.typeArticle-
dc.identifier.doi10.1081/SCC-100107011-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.31, no.23, pp.3627 - 3632-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume31-
dc.citation.number23-
dc.citation.startPage3627-
dc.citation.endPage3632-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000171792400009-
dc.identifier.scopusid2-s2.0-0034770940-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusOXIDATIVE CLEAVAGE-
dc.subject.keywordPlusPEPTIDE-SYNTHESIS-
dc.subject.keywordPlusDIOXIRANE-
dc.subject.keywordPlusCARBONYL-
dc.subject.keywordAuthorhalogenation-
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