Total synthesis of (+)-furanomycin

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dc.contributor.authorKang, SungHoko
dc.contributor.authorLee, SBko
dc.date.accessioned2013-02-27T17:49:03Z-
dc.date.available2013-02-27T17:49:03Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-04-
dc.identifier.citationCHEMICAL COMMUNICATIONS, no.7, pp.761 - 762-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/69927-
dc.description.abstractA highly enantioselective total synthesis of (+)-furanomycin 24 has been achieved via the mercury cation-mediated cyclizations of gamma-hydroxy alkene 4 and homoallylic trichloroacetimidate 11 to install the trans-2,5-disubstituted tetrahydrofuran and the (alpha S)-amino acid side chain, respectively.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subject(+)-POLYOXAMIC ACID-
dc.subjectALLYLIC ALCOHOLS-
dc.subjectFURANOMYCIN-
dc.subjectREARRANGEMENT-
dc.subjectBIOSYNTHESIS-
dc.subjectMECHANISM-
dc.subjectREAGENTS-
dc.subjectROUTES-
dc.titleTotal synthesis of (+)-furanomycin-
dc.typeArticle-
dc.identifier.wosid000073042400015-
dc.type.rimsART-
dc.citation.issue7-
dc.citation.beginningpage761-
dc.citation.endingpage762-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorLee, SB-
dc.type.journalArticleArticle-
dc.subject.keywordPlus(+)-POLYOXAMIC ACID-
dc.subject.keywordPlusALLYLIC ALCOHOLS-
dc.subject.keywordPlusFURANOMYCIN-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusREAGENTS-
dc.subject.keywordPlusROUTES-
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