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dc.contributor.authorLee, YS-
dc.contributor.authorLee, JY-
dc.contributor.authorJeong, JH-
dc.contributor.authorPark, H-
dc.date.accessioned2024-01-21T18:15:09Z-
dc.date.available2024-01-21T18:15:09Z-
dc.date.created2021-09-05-
dc.date.issued1997-06-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143771-
dc.description.abstractAn efficient synthesis of 3-(E)-hydroxy- and 3-(E)-acetoxypropenylcephem derivatives, key intermediates for the synthesis of 3-(E)-propenylcephalosporins was achieved via Stille coupling reaction of 3-trifloxycephem with 3-(E)-tributylstannylallylic alcohol.-
dc.languageEnglish-
dc.publisherPHARMACEUTICAL SOCIETY KOREA-
dc.subjectCEPHALOSPORINS-
dc.titleAn efficient synthesis of 3-(E)-hydroxypropenyl cephem derivatives, key intermediates for 3-(E)-ammoniopropenylcephalosporin antibiotics-
dc.typeArticle-
dc.identifier.doi10.1007/BF02976160-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIVES OF PHARMACAL RESEARCH, v.20, no.3, pp.288 - 290-
dc.citation.titleARCHIVES OF PHARMACAL RESEARCH-
dc.citation.volume20-
dc.citation.number3-
dc.citation.startPage288-
dc.citation.endPage290-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997XG35500016-
dc.identifier.scopusid2-s2.0-20544476152-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusCEPHALOSPORINS-
dc.subject.keywordAuthorammoniopropenyl-
dc.subject.keywordAuthor3-(E)-propenylcephem-
dc.subject.keywordAuthorcephalosporins-
dc.subject.keywordAuthorantibacterial-
dc.subject.keywordAuthorStille coupling-
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