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

Enantioselective conjugate radical addition to alpha '-hydroxy enones

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dc.contributor.authorLee, Sunggiko
dc.contributor.authorLim, Chae Joko
dc.contributor.authorKim, Sung Gakko
dc.contributor.authorSubramaniam, Rajeshko
dc.contributor.authorZimmerman, Jakeko
dc.contributor.authorSibi, Mukund P.ko
dc.date.accessioned2013-03-06T15:17:04Z-
dc.date.available2013-03-06T15:17:04Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-09-
dc.identifier.citationORGANIC LETTERS, v.8, no.19, pp.4311 - 4313-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10203/87390-
dc.description.abstractEnantioselective conjugate radical addition to alpha '-hydroxy alpha,beta-unsaturated ketones, compounds containing bidentate donors, has been investigated. It has been found that radical additions to alpha '-hydroxy alpha,beta-unsaturated ketones in the presence of Mg(NTf2)(2) and bisoxazoline ligand 5a proceeded cleanly, yielding the addition products in high chemical yields and good enantiomeric excesses.-
dc.languageEnglish-
dc.publisherAmer Chemical Soc-
dc.subjectCHIRAL LEWIS-ACID-
dc.subjectCATALYSIS-
dc.subjectALKYLATIONS-
dc.titleEnantioselective conjugate radical addition to alpha '-hydroxy enones-
dc.typeArticle-
dc.identifier.wosid000240339700035-
dc.identifier.scopusid2-s2.0-33749007119-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.issue19-
dc.citation.beginningpage4311-
dc.citation.endingpage4313-
dc.citation.publicationnameORGANIC LETTERS-
dc.identifier.doi10.1021/ol061634z-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorLee, Sunggi-
dc.contributor.nonIdAuthorLim, Chae Jo-
dc.contributor.nonIdAuthorSubramaniam, Rajesh-
dc.contributor.nonIdAuthorZimmerman, Jake-
dc.contributor.nonIdAuthorSibi, Mukund P.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCHIRAL LEWIS-ACID-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusALKYLATIONS-
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