Palladium-catalyzed arylation of alpha,beta-unsaturated Weinreb amides

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dc.contributor.authorK H Kim-
dc.contributor.authorSangku Lee-
dc.contributor.authorS H Kim-
dc.contributor.authorC H Lim-
dc.contributor.authorJ N Kim-
dc.date.accessioned2017-04-19T09:33:10Z-
dc.date.available2017-04-19T09:33:10Z-
dc.date.issued2012-
dc.identifier.issn0040-4039-
dc.identifier.uri10.1016/j.tetlet.2012.07.023ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10876-
dc.description.abstractPalladium-catalyzed arylation of α,β-unsaturated Weinreb amides has been examined to obtain β-aryl-α,β-unsaturated Weinreb amides. The chelation between the palladium center of an alkylpalladium intermediate and Weinreb amide moiety facilitated both coordination and insertion steps.-
dc.publisherElsevier-
dc.titlePalladium-catalyzed arylation of alpha,beta-unsaturated Weinreb amides-
dc.title.alternativePalladium-catalyzed arylation of alpha,beta-unsaturated Weinreb amides-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number38-
dc.citation.endPage5093-
dc.citation.startPage5088-
dc.citation.volume53-
dc.contributor.affiliatedAuthorSangku Lee-
dc.contributor.alternativeName김고훈-
dc.contributor.alternativeName이상구-
dc.contributor.alternativeName김세희-
dc.contributor.alternativeName임철희-
dc.contributor.alternativeName김재녕-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 53, no. 38, pp. 5088-5093-
dc.identifier.doi10.1016/j.tetlet.2012.07.023-
dc.subject.keywordArylation-
dc.subject.keywordChelation-
dc.subject.keywordPalladium-
dc.subject.keywordWeinreb amides-
dc.subject.localArylation-
dc.subject.localChelation-
dc.subject.localPalladium-
dc.subject.localWeinreb amides-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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