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dc.contributor.authorLEE, E-
dc.contributor.authorHUR, CU-
dc.contributor.authorJEONG, YC-
dc.contributor.authorRHEE, YH-
dc.contributor.authorCHANG, MH-
dc.date.accessioned2024-01-21T23:40:44Z-
dc.date.available2024-01-21T23:40:44Z-
dc.date.created2022-01-10-
dc.date.issued1991-09-15-
dc.identifier.issn0022-4936-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/146734-
dc.description.abstractE-alpha-Arylidene-gamma-butyrolactones were prepared by the radical addition-elimination reaction of Z-alpha-stannylmethylene-gamma-butyrolactones, whereas the palladium(0) catalysed cross-coupling reaction of the same substrates afforded Z-alpha-arylidene-gamma-butyrolactones.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectCYCLIZATION-
dc.subjectELIMINATION-
dc.subjectARYLATION-
dc.titlePREPARATION OF E-ALPHA-ARYLIDENE-GAMMA-BUTYROLACTONES AND Z-ALPHA-ARYLIDENE-GAMMA-BUTYROLACTONES FROM Z-ALPHA-STANNYLMETHYLENE-GAMMA-BUTYROLACTONES - STEREOSELECTIVE SYNTHESIS OF (+/-)-SAVININ AND (+/-)-GADAIN-
dc.typeArticle-
dc.identifier.doi10.1039/c39910001314-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, no.18, pp.1314 - 1315-
dc.citation.titleJOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS-
dc.citation.number18-
dc.citation.startPage1314-
dc.citation.endPage1315-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1991GH46000049-
dc.identifier.scopusid2-s2.0-0025823022-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusELIMINATION-
dc.subject.keywordPlusARYLATION-
dc.subject.keywordAuthorstereoselective-
dc.subject.keywordAuthorsalvinin-
dc.subject.keywordAuthorgadain-
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