Direct one-pot introduction of 2-methylpyridines to Baylis-Hillman adducts via base-mediated 3-aza-Cope rearrangement

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dc.contributor.authorH S Lee-
dc.contributor.authorSangku Lee-
dc.contributor.authorS H Kim-
dc.contributor.authorJ N Kim-
dc.date.accessioned2017-04-19T09:25:26Z-
dc.date.available2017-04-19T09:25:26Z-
dc.date.issued2011-
dc.identifier.issn00404039-
dc.identifier.uri10.1016/j.tetlet.2011.07.101ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10347-
dc.description.abstractAn efficient and regioselective introduction method of 2-methylpyridines to the secondary position of Baylis-Hillman adducts has been developed. A base treatment of 2-methylpyridinium salt of Baylis-Hillman bromide generated N-allylenamine intermediate which underwent a facile 3-aza-Cope rearrangement under mild conditions to produce the product.-
dc.publisherElsevier-
dc.titleDirect one-pot introduction of 2-methylpyridines to Baylis-Hillman adducts via base-mediated 3-aza-Cope rearrangement-
dc.title.alternativeDirect one-pot introduction of 2-methylpyridines to Baylis-Hillman adducts via base-mediated 3-aza-Cope rearrangement-
dc.typeArticle-
dc.citation.titleTetrahedron Letters-
dc.citation.number39-
dc.citation.endPage5042-
dc.citation.startPage5039-
dc.citation.volume52-
dc.contributor.affiliatedAuthorSangku Lee-
dc.contributor.alternativeName이현승-
dc.contributor.alternativeName이상구-
dc.contributor.alternativeName김세희-
dc.contributor.alternativeName김재녕-
dc.identifier.bibliographicCitationTetrahedron Letters, vol. 52, no. 39, pp. 5039-5042-
dc.identifier.doi10.1016/j.tetlet.2011.07.101-
dc.subject.keyword2-Methylpyridines-
dc.subject.keywordAza-Cope rearrangement-
dc.subject.keywordBaylis-Hillman adducts-
dc.subject.local2-Methylpyridines-
dc.subject.localAza-Cope rearrangement-
dc.subject.localBaylis-Hillman adducts-
dc.subject.localbaylis-hillman adducts-
dc.description.journalClassY-
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Ochang Branch Institute > Anticancer Agent Research Center > 1. Journal Articles
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