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dc.contributor.authorChoi, HY-
dc.contributor.authorLee, BS-
dc.contributor.authorChi, DY-
dc.contributor.authorKim, DJ-
dc.date.accessioned2024-01-21T16:13:58Z-
dc.date.available2024-01-21T16:13:58Z-
dc.date.created2021-09-03-
dc.date.issued1998-12-01-
dc.identifier.issn0385-5414-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142649-
dc.description.abstractKey intermediates for potential antitumor or antifungal agents, 2- and 3-methyl-6,7-dibromoquinoline-5,8-diones have been synthesized from 2,5-dimethoxyaniline and acrolein derivatives in three-step-one-pot with 38-41% isolation yields using Skraup reaction. The three steps are ring formation of quinoline, didemethylation, and oxidation of hydroquinone including dibromination on C6 and C7 positions.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectLAVENDAMYCIN METHYL-ESTER-
dc.subjectDIELS-ALDER REACTIONS-
dc.subjectSTREPTONIGRIN-
dc.subjectSYSTEM-
dc.titleNew efficient syntheses of 6,7-dibromoquinoline-5,8-diones-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationHETEROCYCLES, v.48, no.12, pp.2647 - 2652-
dc.citation.titleHETEROCYCLES-
dc.citation.volume48-
dc.citation.number12-
dc.citation.startPage2647-
dc.citation.endPage2652-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000077840900022-
dc.identifier.scopusid2-s2.0-0000671180-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusLAVENDAMYCIN METHYL-ESTER-
dc.subject.keywordPlusDIELS-ALDER REACTIONS-
dc.subject.keywordPlusSTREPTONIGRIN-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordAuthorskraup reaction-
dc.subject.keywordAuthorquinolinediones-
dc.subject.keywordAuthorsodium chlorate-
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