Vinylogous N,N-dimethylaminomethylenation of 3-[(1-substituted)ethylidene]- oxindoles with N,N-dimethylformamide dimethylacetal

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dc.contributor.authorH J Lee-
dc.contributor.authorSangku Lee-
dc.contributor.authorJ Yu-
dc.contributor.authorJ N Kim-
dc.date.accessioned2017-04-19T09:52:47Z-
dc.date.available2017-04-19T09:52:47Z-
dc.date.issued2014-
dc.identifier.issn0040-4039-
dc.identifier.uri10.1016/j.tetlet.2014.02.130ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11951-
dc.description.abstractAn efficient stereoselective synthesis of various 3-(3-dimethylaminoprop-2- enylidene)oxindoles has been disclosed. The compounds were synthesized via a vinylogous N,N-dimethylaminomethylenation at the γ-position of 3-[(1-substituted)ethylidene]oxindoles with DMF-DMA.-
dc.publisherElsevier-
dc.titleVinylogous N,N-dimethylaminomethylenation of 3-[(1-substituted)ethylidene]- oxindoles with N,N-dimethylformamide dimethylacetal-
dc.title.alternativeVinylogous N,N-dimethylaminomethylenation of 3-[(1-substituted)ethylidene]- oxindoles with N,N-dimethylformamide dimethylacetal-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number15-
dc.citation.endPage2454-
dc.citation.startPage2450-
dc.citation.volume55-
dc.contributor.affiliatedAuthorSangku Lee-
dc.contributor.alternativeName이현주-
dc.contributor.alternativeName이상구-
dc.contributor.alternativeName유진-
dc.contributor.alternativeName김재녕-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 55, no. 15, pp. 2450-2454-
dc.identifier.doi10.1016/j.tetlet.2014.02.130-
dc.subject.keyword3-Alkylideneoxindoles-
dc.subject.keywordDMF-DMA-
dc.subject.keywordStereoselective-
dc.subject.keywordVinylogous N,N-dimethylaminomethylenation-
dc.subject.local3-Alkylideneoxindoles-
dc.subject.localDMF-DMA-
dc.subject.localStereo-selective-
dc.subject.localStereoselective-
dc.subject.localVinylogous N,N-dimethylaminomethylenation-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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