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

A stereocontrolled synthetic route to anti-beta-amino alcohols

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dc.contributor.authorKang, SungHoko
dc.contributor.authorHwang, YSko
dc.contributor.authorYoun, JHko
dc.date.accessioned2013-03-03T12:13:27Z-
dc.date.available2013-03-03T12:13:27Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-10-
dc.identifier.citationTETRAHEDRON LETTERS, v.42, no.43, pp.7599 - 7603-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/78616-
dc.description.abstractA physiologically indispensable beta -amino hydroxy functionality has been constructed with complete anti-stereoselectivity by intramolecular iodoamidation of (Z)-olefinic homoallylic trichloroacetimidates 4-6, 18, 20, 30 and 32, which comprise bulky substituents at the vinylic positions. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subjectENANTIOCONTROLLED SYNTHESIS-
dc.subjectENANTIOSELECTIVE SYNTHESIS-
dc.subjectACIDS-
dc.subjectCOMPLEXES-
dc.subjectCATALYST-
dc.subjectESTERS-
dc.titleA stereocontrolled synthetic route to anti-beta-amino alcohols-
dc.typeArticle-
dc.identifier.wosid000171556600017-
dc.identifier.scopusid2-s2.0-0035935116-
dc.type.rimsART-
dc.citation.volume42-
dc.citation.issue43-
dc.citation.beginningpage7599-
dc.citation.endingpage7603-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorHwang, YS-
dc.contributor.nonIdAuthorYoun, JH-
dc.type.journalArticleArticle-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusENANTIOCONTROLLED SYNTHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusACIDS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusCATALYST-
dc.subject.keywordPlusESTERS-
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CH-Journal Papers(저널논문)
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