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

An enantiocontrolled synthesis of pyrrolizidines, (-)-platynecine and (-)-hadinecine

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dc.contributor.authorKang, SungHoko
dc.contributor.authorKim, GTko
dc.contributor.authorYoo, YSko
dc.date.accessioned2013-03-02T20:21:18Z-
dc.date.available2013-03-02T20:21:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1997-01-
dc.identifier.citationTETRAHEDRON LETTERS, v.38, no.4, pp.603 - 606-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/75358-
dc.description.abstractTrisubstituted allylic alcohols 13 and 14 have been converted into a single isomeric trans-oxazoline 16 via an intramolecular iodoamidation of the corresponding trichloroacetimidates, which have been elaborated into (-)-platynecine 1 and (-)-hadinecine 2 via a common intermediate pyrrolizidine 3. (C) 1997, Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectENANTIOSELECTIVE SYNTHESIS-
dc.subjectRADICAL CYCLIZATIONS-
dc.subjectALKALOIDS-
dc.subject(+)-HELIOTRIDINE-
dc.subject(+)-RETRONECINE-
dc.subjectDIHYDROXYHELIOTRIDANE-
dc.subjectPRECURSOR-
dc.subjectAMINE-
dc.subjectACID-
dc.titleAn enantiocontrolled synthesis of pyrrolizidines, (-)-platynecine and (-)-hadinecine-
dc.typeArticle-
dc.identifier.wosidA1997WD98800027-
dc.identifier.scopusid2-s2.0-0031013935-
dc.type.rimsART-
dc.citation.volume38-
dc.citation.issue4-
dc.citation.beginningpage603-
dc.citation.endingpage606-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorKim, GT-
dc.contributor.nonIdAuthorYoo, YS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusRADICAL CYCLIZATIONS-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlus(+)-HELIOTRIDINE-
dc.subject.keywordPlus(+)-RETRONECINE-
dc.subject.keywordPlusDIHYDROXYHELIOTRIDANE-
dc.subject.keywordPlusPRECURSOR-
dc.subject.keywordPlusAMINE-
dc.subject.keywordPlusACID-
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