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dc.contributor.authorHahn, HG-
dc.contributor.authorChang, KH-
dc.contributor.authorLee, WS-
dc.contributor.authorYoo, JU-
dc.date.accessioned2024-01-21T19:10:35Z-
dc.date.available2024-01-21T19:10:35Z-
dc.date.created2022-01-10-
dc.date.issued1996-11-
dc.identifier.issn0022-152X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144251-
dc.description.abstractA synthesis of new dihydrooxathiinoquinoline 4 is described. The key compound 6 was prepared by known methods from acetoacetanilide 1. A condensation of beta-chlorosulfide 6 in 75% aqueous sulfuric acid gave quinolone 5. Conversion of 5 to 4 was achieved by treatment with potassium hydroxide in ethanol solution.-
dc.languageEnglish-
dc.publisherHETERO CORPORATION-
dc.titleSynthesis of new dihydrooxathiino[2,3-b]quinoline-
dc.typeArticle-
dc.identifier.doi10.1002/jhet.5570330681-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF HETEROCYCLIC CHEMISTRY, v.33, no.6, pp.2055 - 2057-
dc.citation.titleJOURNAL OF HETEROCYCLIC CHEMISTRY-
dc.citation.volume33-
dc.citation.number6-
dc.citation.startPage2055-
dc.citation.endPage2057-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996WE32000081-
dc.identifier.scopusid2-s2.0-2742529154-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
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