pubmed-article:15151408 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C1511695 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C1704419 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C1122839 | lld:lifeskim |
pubmed-article:15151408 | lifeskim:mentions | umls-concept:C1505891 | lld:lifeskim |
pubmed-article:15151408 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:15151408 | pubmed:dateCreated | 2004-5-20 | lld:pubmed |
pubmed-article:15151408 | pubmed:abstractText | A 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 |
pubmed-article:15151408 | pubmed:language | eng | lld:pubmed |
pubmed-article:15151408 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15151408 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15151408 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15151408 | pubmed:month | May | lld:pubmed |
pubmed-article:15151408 | pubmed:issn | 1523-7060 | lld:pubmed |
pubmed-article:15151408 | pubmed:author | pubmed-author:NaitoTakeakiT | lld:pubmed |
pubmed-article:15151408 | pubmed:author | pubmed-author:MiyataOkikoO | lld:pubmed |
pubmed-article:15151408 | pubmed:author | pubmed-author:TakedaNorihik... | lld:pubmed |
pubmed-article:15151408 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15151408 | pubmed:day | 27 | lld:pubmed |
pubmed-article:15151408 | pubmed:volume | 6 | lld:pubmed |
pubmed-article:15151408 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15151408 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15151408 | pubmed:pagination | 1761-3 | lld:pubmed |
pubmed-article:15151408 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:meshHeading | pubmed-meshheading:15151408... | lld:pubmed |
pubmed-article:15151408 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:15151408 | pubmed:articleTitle | Highly effective synthetic methods for substituted 2-arylbenzofurans using [3,3]-sigmatropic rearrangement: short syntheses of stemofuran a and eupomatenoid 6. | lld:pubmed |
pubmed-article:15151408 | pubmed:affiliation | Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan. | lld:pubmed |
pubmed-article:15151408 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:15151408 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |