An expedient synthesis of oxindole dimers by direct oxidative dimerization of oxindoles

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dc.contributor.authorH J Lee-
dc.contributor.authorSangku Lee-
dc.contributor.authorJ W Lim-
dc.contributor.authorJ N Kim-
dc.date.accessioned2017-04-19T09:42:45Z-
dc.date.available2017-04-19T09:42:45Z-
dc.date.issued2013-
dc.identifier.issn0253-2964-
dc.identifier.uri10.5012/bkcs.2013.34.8.2446ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11504-
dc.description.abstractOxindole dimers have been used as intermediates in the synthesis of various cyclotryptamine alkaloids. An efficient direct synthesis of oxindole dimers has been carried out from 3-substituted oxindoles via an oxidative dimerization using manganese(III) acetate or copper acetate/silver acetate system.-
dc.publisherWiley-
dc.titleAn expedient synthesis of oxindole dimers by direct oxidative dimerization of oxindoles-
dc.title.alternativeAn expedient synthesis of oxindole dimers by direct oxidative dimerization of oxindoles-
dc.typeArticle-
dc.citation.titleBulletin of Korean Chemical Society-
dc.citation.number8-
dc.citation.endPage2450-
dc.citation.startPage2446-
dc.citation.volume34-
dc.contributor.affiliatedAuthorSangku Lee-
dc.contributor.alternativeName이현주-
dc.contributor.alternativeName이상구-
dc.contributor.alternativeName임진우-
dc.contributor.alternativeName김재녕-
dc.identifier.bibliographicCitationBulletin of Korean Chemical Society, vol. 34, no. 8, pp. 2446-2450-
dc.identifier.doi10.5012/bkcs.2013.34.8.2446-
dc.subject.keywordManganese(III) acetate-
dc.subject.keywordOxidative dimerization-
dc.subject.keywordOxindole dimers-
dc.subject.keywordOxindoles-
dc.subject.localManganese(III) acetate-
dc.subject.localOxidative dimerization-
dc.subject.localOxindole dimers-
dc.subject.localOxindoles-
dc.subject.localOxindole-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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