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pubmed-article:15151408pubmed:dateCreated2004-5-20lld:pubmed
pubmed-article:15151408pubmed:abstractTextA new and efficient synthesis of 2-arylbenzofurans has been achieved via a route involving acylation and subsequent [3,3]-sigmatropic rearrangement of oxime ethers. Its synthetic utility is demonstrated by a short synthesis of stemofuran A and eupomatenoid 6 in which no procedure for protection of the phenolic hydroxyl groups is needed. [reaction--see text]lld:pubmed
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pubmed-article:15151408pubmed:authorpubmed-author:NaitoTakeakiTlld:pubmed
pubmed-article:15151408pubmed:authorpubmed-author:MiyataOkikoOlld:pubmed
pubmed-article:15151408pubmed:authorpubmed-author:TakedaNorihik...lld:pubmed
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pubmed-article:15151408pubmed:pagination1761-3lld:pubmed
pubmed-article:15151408pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15151408pubmed:year2004lld:pubmed
pubmed-article:15151408pubmed:articleTitleHighly effective synthetic methods for substituted 2-arylbenzofurans using [3,3]-sigmatropic rearrangement: short syntheses of stemofuran a and eupomatenoid 6.lld:pubmed
pubmed-article:15151408pubmed:affiliationKobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan.lld:pubmed
pubmed-article:15151408pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15151408pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed