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dc.contributor.authorKang, HY-
dc.contributor.authorLee, SH-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.date.accessioned2024-01-21T19:11:34Z-
dc.date.available2024-01-21T19:11:34Z-
dc.date.created2021-09-05-
dc.date.issued1996-10-14-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144268-
dc.description.abstractAn efficient synthetic route for cephalosporin derivatives with various substituents at the 3-position has been developed It involves cycloaddition with silyl enol ethers or silylketene acetals followed by fragmentation utilizing the 3-cephem triflate 1 as a starting material. Copyright (C) 1996 Elsevier Science Ltd-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleSynthesis of cephalosporin derivatives utilizing the cephem triflate .1. introduction of 3-position substituents via a cycloaddition-fragmentation route-
dc.typeArticle-
dc.identifier.doi10.1016/0040-4039(96)01714-5-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.37, no.42, pp.7549 - 7552-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume37-
dc.citation.number42-
dc.citation.startPage7549-
dc.citation.endPage7552-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996VL99300022-
dc.identifier.scopusid2-s2.0-0030583480-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthorcycloaddition-
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