pubmed-article:18200590 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0003209 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0034325 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0008562 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C1515999 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0449830 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0205344 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C2827597 | lld:lifeskim |
pubmed-article:18200590 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
pubmed-article:18200590 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:18200590 | pubmed:dateCreated | 2008-5-5 | lld:pubmed |
pubmed-article:18200590 | pubmed:abstractText | The assignment of the absolute configuration of novel anti-inflammatory pyrrole derivatives has been accomplished by a combined strategy based on independent physical methods. The key step of our stereochemical characterization approach is the production at mg-scale of enantiomerically pure forms by HPLC on Chiralpak IA stationary phase. | lld:pubmed |
pubmed-article:18200590 | pubmed:language | eng | lld:pubmed |
pubmed-article:18200590 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18200590 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18200590 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18200590 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18200590 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18200590 | pubmed:month | Jun | lld:pubmed |
pubmed-article:18200590 | pubmed:issn | 1520-636X | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:FerrettiRosel... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:VillaniClaudi... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:La... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:BiavaMariange... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:PorrettaGiuli... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:CirilliRobert... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:GallinellaBru... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:FaresVincenzo... | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:PoceGiovannaG | lld:pubmed |
pubmed-article:18200590 | pubmed:author | pubmed-author:SupinoSibilla... | lld:pubmed |
pubmed-article:18200590 | pubmed:copyrightInfo | (c) 2008 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:18200590 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18200590 | pubmed:volume | 20 | lld:pubmed |
pubmed-article:18200590 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18200590 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18200590 | pubmed:pagination | 775-80 | lld:pubmed |
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pubmed-article:18200590 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18200590 | pubmed:articleTitle | HPLC enantioseparation and absolute configuration of novel anti-inflammatory pyrrole derivatives. | lld:pubmed |
pubmed-article:18200590 | pubmed:affiliation | Università La Sapienza, Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, 00185 Rome, Italy. | lld:pubmed |
pubmed-article:18200590 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18200590 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |