Tin-free radical carbonylation: Synthesis of acylated oxime ethers using alkyl allyl sulfone precursors, carbon monoxide, and phenylsulfonyl oxime ether

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dc.contributor.authorKim, Sangmoko
dc.contributor.authorLim, Kyoung-Chanko
dc.contributor.authorKim, Sung Gakko
dc.contributor.authorRyu, Ilhyongko
dc.date.accessioned2013-03-07T07:40:43Z-
dc.date.available2013-03-07T07:40:43Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2007-
dc.identifier.citationADVANCED SYNTHESIS & CATALYSIS, v.349, no.4-5, pp.527 - 530-
dc.identifier.issn1615-4150-
dc.identifier.urihttp://hdl.handle.net/10203/89719-
dc.description.abstractAcylated oxime ethers have been prepared by a three-component coupling reaction using alkyl allyl sulfone precursors, carbon monoxide, and phenylsulfonyl oxime ether derivatives under tin-free radical reaction conditions.-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.subjectTHIOHYDROXAMATE ESTERS-
dc.subjectRATE CONSTANTS-
dc.subjectIODIDES-
dc.titleTin-free radical carbonylation: Synthesis of acylated oxime ethers using alkyl allyl sulfone precursors, carbon monoxide, and phenylsulfonyl oxime ether-
dc.typeArticle-
dc.identifier.wosid000245379400008-
dc.identifier.scopusid2-s2.0-34547214901-
dc.type.rimsART-
dc.citation.volume349-
dc.citation.issue4-5-
dc.citation.beginningpage527-
dc.citation.endingpage530-
dc.citation.publicationnameADVANCED SYNTHESIS & CATALYSIS-
dc.identifier.doi10.1002/adsc.200600500-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorKim, Sangmo-
dc.contributor.nonIdAuthorLim, Kyoung-Chan-
dc.contributor.nonIdAuthorRyu, Ilhyong-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcarbonylation-
dc.subject.keywordAuthorradical reactions-
dc.subject.keywordAuthorradicals-
dc.subject.keywordAuthorsynthetic methods-
dc.subject.keywordPlusTHIOHYDROXAMATE ESTERS-
dc.subject.keywordPlusRATE CONSTANTS-
dc.subject.keywordPlusIODIDES-
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