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

A versatile synthetic route to indolizidines, (+)-7-deoxy-6-epicastanospermine, (-)-7,8-dideoxy-6-epicastanospermine and (-)-N-acetylslaframine

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dc.contributor.authorKang, SungHoko
dc.contributor.authorKim, JSko
dc.contributor.authorYoun, JHko
dc.date.accessioned2013-03-02T20:17:32Z-
dc.date.available2013-03-02T20:17:32Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-12-
dc.identifier.citationTETRAHEDRON LETTERS, v.39, no.49, pp.9047 - 9050-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/75325-
dc.description.abstract(+)-7-Deoxy-6-epicastanospermine 1, (-)-7,8-dideoxy-6-epicastanospermine 2 and (-)-N-acetylslaframine 4 have been synthesized via the stereoselective intramolecular iodocyclization of trichloroacetimidates generated from cis-olefinic allylic alcohols 7 and 15, respectively. (C) 1998 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectENANTIOCONTROLLED SYNTHESIS-
dc.subject(-)-SLAFRAMINE-
dc.subjectALKALOIDS-
dc.subjectSWAINSONINE-
dc.subjectSLAFRAMINE-
dc.titleA versatile synthetic route to indolizidines, (+)-7-deoxy-6-epicastanospermine, (-)-7,8-dideoxy-6-epicastanospermine and (-)-N-acetylslaframine-
dc.typeArticle-
dc.identifier.wosid000077080000033-
dc.identifier.scopusid2-s2.0-0032481080-
dc.type.rimsART-
dc.citation.volume39-
dc.citation.issue49-
dc.citation.beginningpage9047-
dc.citation.endingpage9050-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorKim, JS-
dc.contributor.nonIdAuthorYoun, JH-
dc.type.journalArticleArticle-
dc.subject.keywordPlusENANTIOCONTROLLED SYNTHESIS-
dc.subject.keywordPlus(-)-SLAFRAMINE-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusSWAINSONINE-
dc.subject.keywordPlusSLAFRAMINE-
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CH-Journal Papers(저널논문)
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