pubmed-article:21456515 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21456515 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
pubmed-article:21456515 | lifeskim:mentions | umls-concept:C0444669 | lld:lifeskim |
pubmed-article:21456515 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:21456515 | lifeskim:mentions | umls-concept:C0056789 | lld:lifeskim |
pubmed-article:21456515 | lifeskim:mentions | umls-concept:C0075804 | lld:lifeskim |
pubmed-article:21456515 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:21456515 | pubmed:dateCreated | 2011-4-29 | lld:pubmed |
pubmed-article:21456515 | pubmed:abstractText | A rapid approach to the spirocyclic core of cyclopamine was achieved in four steps from 2-pentenyl-furan. A furan Diels-Alder reaction followed by a one-pot dehalogenation/amination sequence provides the oxabicyclic triene that upon treatment with Grubbs' catalyst undergoes smooth rearrangement to the tricyclic core. | lld:pubmed |
pubmed-article:21456515 | pubmed:language | eng | lld:pubmed |
pubmed-article:21456515 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21456515 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21456515 | pubmed:month | May | lld:pubmed |
pubmed-article:21456515 | pubmed:issn | 1523-7052 | lld:pubmed |
pubmed-article:21456515 | pubmed:author | pubmed-author:WrightDennis... | lld:pubmed |
pubmed-article:21456515 | pubmed:author | pubmed-author:OblakE... | lld:pubmed |
pubmed-article:21456515 | pubmed:author | pubmed-author:G-DayanandanN... | lld:pubmed |
pubmed-article:21456515 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21456515 | pubmed:day | 6 | lld:pubmed |
pubmed-article:21456515 | pubmed:volume | 13 | lld:pubmed |
pubmed-article:21456515 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21456515 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21456515 | pubmed:pagination | 2433-5 | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:meshHeading | pubmed-meshheading:21456515... | lld:pubmed |
pubmed-article:21456515 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21456515 | pubmed:articleTitle | Tandem metathesis reactions of oxabicyclo[2.2.1]heptenes: studies on the spirocyclic core of cyclopamine. | lld:pubmed |
pubmed-article:21456515 | pubmed:affiliation | Department of Pharmaceutical Sciences, University of Connecticut, Storrs, Connecticut 06269, United States. | lld:pubmed |
pubmed-article:21456515 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21456515 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |