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dc.contributor.authorKIM, SH-
dc.contributor.authorKIM, K-
dc.contributor.authorKIM, J-
dc.contributor.authorKIM, K-
dc.contributor.authorKIM, JH-
dc.date.accessioned2024-01-21T22:31:20Z-
dc.date.available2024-01-21T22:31:20Z-
dc.date.created2021-09-02-
dc.date.issued1993-07-
dc.identifier.issn0022-152X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/146024-
dc.description.abstractThe reactions of 2-alkyl-5-phenylisothiazole-3-thiones with 2-chloro-1,3-dicarbonyl compounds in chloroform gave the corresponding isothiazolium chlorides which, upon treatment at room temperature with sodium borohydride in a mixture of chloroform and ethanol, underwent S-N bond cleavage to give 3-alkyl-4,5-disubstituted-2-thiophenacylidenethiazolines. Similarly, treatment of the isothiazolium chlorides with triphenylphosphite in chloroform at 60-degrees afforded the same thiazoline derivatives.-
dc.languageEnglish-
dc.publisherHETERO CORPORATION-
dc.titleA FACILE METHOD FOR 2-THIOPHENACYLIDENETHIAZOLINE DERIVATIVES-
dc.typeArticle-
dc.identifier.doi10.1002/jhet.5570300415-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF HETEROCYCLIC CHEMISTRY, v.30, no.4, pp.929 - 938-
dc.citation.titleJOURNAL OF HETEROCYCLIC CHEMISTRY-
dc.citation.volume30-
dc.citation.number4-
dc.citation.startPage929-
dc.citation.endPage938-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1993MD59700015-
dc.identifier.scopusid2-s2.0-0000513016-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthortriphenylphosphite-
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