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College of Engineering(공과대학)Dept. of Nuclear and Quantum Engineering(원자력및양자공학과)NE-Journal Papers(저널논문)

A STEREOCONTROLLED SYNTHESIS OF A KEY INTERMEDIATE TO (+)-THIENAMYCIN

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dc.contributor.authorKang, SungHoko
dc.contributor.authorKIM, WJko
dc.date.accessioned2013-02-24T09:28:55Z-
dc.date.available2013-02-24T09:28:55Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1991-07-
dc.identifier.citationSYNLETT, no.7, pp.520 - 522-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/56078-
dc.description.abstractA formal synthesis of (+)-thienamycin was achieved by the enantioselective preparation of key intermediate azetidinone 2 [benzyl (2R,3S)-3-{(S)-1-hydroxyethyl}-4-oxo-2-azetidineacetate] via an intramolecular nitrone 1,3-dipolar cycloaddition.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG-
dc.subjectDEHYDROPEPTIDASE-I-
dc.subjectRENAL DIPEPTIDASE-
dc.subjectTHIENAMYCIN-
dc.subjectANTIBIOTICS-
dc.subjectOXIDATION-
dc.subjectACIDS-
dc.titleA STEREOCONTROLLED SYNTHESIS OF A KEY INTERMEDIATE TO (+)-THIENAMYCIN-
dc.typeArticle-
dc.identifier.wosidA1991FV76200028-
dc.type.rimsART-
dc.citation.issue7-
dc.citation.beginningpage520-
dc.citation.endingpage522-
dc.citation.publicationnameSYNLETT-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorKIM, WJ-
dc.type.journalArticleNote-
dc.subject.keywordPlusDEHYDROPEPTIDASE-I-
dc.subject.keywordPlusRENAL DIPEPTIDASE-
dc.subject.keywordPlusTHIENAMYCIN-
dc.subject.keywordPlusANTIBIOTICS-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusACIDS-
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CH-Journal Papers(저널논문)
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