| pubmed-article:21671636 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0524465 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0444669 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0294188 | lld:lifeskim |
| pubmed-article:21671636 | lifeskim:mentions | umls-concept:C0917735 | lld:lifeskim |
| pubmed-article:21671636 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:21671636 | pubmed:dateCreated | 2011-7-8 | lld:pubmed |
| pubmed-article:21671636 | pubmed:abstractText | Regio-, stereo-, and facial selective [4 + 2] cycloadditions between highly activated vinyl sulfones and 1,3-dienes derived from (R)-4-tert-butyldimethylsilyloxy-2-cyclohexen-1-one provide a powerful approach for the asymmetric synthesis of compounds containing the bicyclo[2.2.2]octanone carbon skeleton. This new methodology has been successfully applied to the asymmetric synthesis of the cis-decalin core structure of the potent anticancer marine natural products superstolides A and B. | lld:pubmed |
| pubmed-article:21671636 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21671636 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21671636 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21671636 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:21671636 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:21671636 | pubmed:author | pubmed-author:HuaZhengmaoZ | lld:pubmed |
| pubmed-article:21671636 | pubmed:author | pubmed-author:JinZhendongZ | lld:pubmed |
| pubmed-article:21671636 | pubmed:author | pubmed-author:ChenLeiL | lld:pubmed |
| pubmed-article:21671636 | pubmed:author | pubmed-author:LiGangqinG | lld:pubmed |
| pubmed-article:21671636 | pubmed:copyrightInfo | © 2011 American Chemical Society | lld:pubmed |
| pubmed-article:21671636 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21671636 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:21671636 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:21671636 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21671636 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21671636 | pubmed:pagination | 3580-3 | lld:pubmed |
| pubmed-article:21671636 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:meshHeading | pubmed-meshheading:21671636... | lld:pubmed |
| pubmed-article:21671636 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21671636 | pubmed:articleTitle | Controlling the facial selectivity of asymmetric [4+2] cyclo-additions: a concise synthesis of the cis-decalin core structure of superstolides A and B. | lld:pubmed |
| pubmed-article:21671636 | pubmed:affiliation | Division of Medicinal and Natural Products Chemistry, Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, USA | lld:pubmed |
| pubmed-article:21671636 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21671636 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
