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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction

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dc.contributor.authorChang, Sukbokko
dc.contributor.authorLee, Mko
dc.contributor.authorKim, Sung Gakko
dc.date.accessioned2013-03-03T10:00:16Z-
dc.date.available2013-03-03T10:00:16Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-10-
dc.identifier.citationSYNLETT, no.10, pp.1557 - 1558-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/78292-
dc.description.abstractN-Alkoxyimidoyl bromides have been successfully employed as an efficient organic partner in the Pd-catalyzed Stille coupling reaction with various organotin compounds, and the corresponding O-alkyloximes were obtained in good to excellent yields.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectRADICAL ACYLATION APPROACH-
dc.subjectOXIME ETHERS-
dc.subjectORGANOTIN COMPOUNDS-
dc.subjectPALLADIUM-
dc.subjectCHLORIDES-
dc.titleN-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction-
dc.typeArticle-
dc.identifier.wosid000171453000016-
dc.identifier.scopusid2-s2.0-0034805839-
dc.type.rimsART-
dc.citation.issue10-
dc.citation.beginningpage1557-
dc.citation.endingpage1558-
dc.citation.publicationnameSYNLETT-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.localauthorKim, Sung Gak-
dc.contributor.nonIdAuthorLee, M-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcatalysis-
dc.subject.keywordAuthorcross-coupling-
dc.subject.keywordAuthorpalladium-
dc.subject.keywordAuthorStille reaction-
dc.subject.keywordAuthortin-
dc.subject.keywordPlusRADICAL ACYLATION APPROACH-
dc.subject.keywordPlusOXIME ETHERS-
dc.subject.keywordPlusORGANOTIN COMPOUNDS-
dc.subject.keywordPlusPALLADIUM-
dc.subject.keywordPlusCHLORIDES-
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CH-Journal Papers(저널논문)
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