An efficient indium-mediated 2-bromoallylation of aldehydes at low temperature in aqueous DMF

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dc.contributor.authorY M Kim-
dc.contributor.authorSangku Lee-
dc.contributor.authorS H Kim-
dc.contributor.authorJ N Kim-
dc.date.accessioned2017-04-19T09:23:32Z-
dc.date.available2017-04-19T09:23:32Z-
dc.date.issued2011-
dc.identifier.issn0040-4039-
dc.identifier.uri10.1016/j.tetlet.2011.04.053ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10158-
dc.description.abstractAn efficient synthesis of 2-bromohomoallylic alcohols was carried out via an indium-mediated Barbier-type 2-bromoallylation of aldehydes in moderate yields. The reaction was performed at low temperature (-20 °C) in aqueous DMF in order to minimize decomposition of 2-bromoallylindium reagent to allene.-
dc.publisherElsevier-
dc.titleAn efficient indium-mediated 2-bromoallylation of aldehydes at low temperature in aqueous DMF-
dc.title.alternativeAn efficient indium-mediated 2-bromoallylation of aldehydes at low temperature in aqueous DMF-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number25-
dc.citation.endPage3242-
dc.citation.startPage3240-
dc.citation.volume52-
dc.contributor.affiliatedAuthorSangku Lee-
dc.contributor.alternativeName김유미-
dc.contributor.alternativeName이상구-
dc.contributor.alternativeName김성환-
dc.contributor.alternativeName김재녕-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 52, no. 25, pp. 3240-3242-
dc.identifier.doi10.1016/j.tetlet.2011.04.053-
dc.subject.keyword2-Bromoallylation-
dc.subject.keywordAllene-
dc.subject.keywordBarbier reaction-
dc.subject.keywordIndium-
dc.subject.local2-Bromoallylation-
dc.subject.localAllene-
dc.subject.localbarbier reaction-
dc.subject.localBarbier reaction-
dc.subject.localIndium-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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