In-mediated allylation of alpha-keto esters with allyl halides

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dc.contributor.authorLee, PHko
dc.contributor.authorLee, KYko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2013-03-04T01:46:14Z-
dc.date.available2013-03-04T01:46:14Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-
dc.identifier.citationSYNTHETIC COMMUNICATIONS, v.31, no.20, pp.3189 - 3196-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/10203/81364-
dc.description.abstractThe chemoselective reaction of alpha -keto esters with allyl halides, propargyl bromides, and allenyl bromide using indium metal afforded alpha -hydroxy-gamma,delta -unsaturated esters in good to excellent yields under mild conditions.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectAQUEOUS-MEDIA-
dc.subjectORGANOMETALLIC REACTIONS-
dc.subjectCARBONYL ALLYLATION-
dc.subjectINDIUM-
dc.subjectALDEHYDES-
dc.subjectSELECTIVITY-
dc.subjectACID-
dc.titleIn-mediated allylation of alpha-keto esters with allyl halides-
dc.typeArticle-
dc.identifier.wosid000171245500021-
dc.identifier.scopusid2-s2.0-0034805311-
dc.type.rimsART-
dc.citation.volume31-
dc.citation.issue20-
dc.citation.beginningpage3189-
dc.citation.endingpage3196-
dc.citation.publicationnameSYNTHETIC COMMUNICATIONS-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.nonIdAuthorLee, PH-
dc.contributor.nonIdAuthorLee, KY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusAQUEOUS-MEDIA-
dc.subject.keywordPlusORGANOMETALLIC REACTIONS-
dc.subject.keywordPlusCARBONYL ALLYLATION-
dc.subject.keywordPlusINDIUM-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusSELECTIVITY-
dc.subject.keywordPlusACID-
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