DSpace at KISTKIST Article2002

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dc.contributor.authorChoi, HY-
dc.contributor.authorKim, DW-
dc.contributor.authorChi, DY-
dc.contributor.authorYoon, EY-
dc.contributor.authorKim, DJ-
dc.date.accessioned2024-01-21T10:14:09Z-
dc.date.available2024-01-21T10:14:09Z-
dc.date.created2021-09-01-
dc.date.issued2002-07-26-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139365-
dc.description.abstractSeveral novel 7-alkylamino-2-methylquinoline-5,8-diones (2) were synthesized from 2,5-dimethoxyaniline in five steps via the Skraup reaction followed by demethylations, oxidative bromination, amination, and debromination. We have achieved an unusual hydrobromic acid catalyzed debromination reactions of several 6-bromo-7-alkyl-amino-2-methylquinoline-5,8-diones, giving 7-alkylamino-2-methylquinoline-5,8-diones in good yields.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectSTREPTONIGRIN-
dc.subjectLAVENDAMYCIN-
dc.subjectEFFICIENT-
dc.subjectSYSTEMS-
dc.titlePreparation of 7-alkylamino-2-methylquinoline-5,8-diones-
dc.typeArticle-
dc.identifier.doi10.1021/jo0257039-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF ORGANIC CHEMISTRY, v.67, no.15, pp.5390 - 5393-
dc.citation.titleJOURNAL OF ORGANIC CHEMISTRY-
dc.citation.volume67-
dc.citation.number15-
dc.citation.startPage5390-
dc.citation.endPage5393-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000176918900047-
dc.identifier.scopusid2-s2.0-0037178514-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusSTREPTONIGRIN-
dc.subject.keywordPlusLAVENDAMYCIN-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordAuthorquinolinedione-
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