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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2008-5-5
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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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1520-636X
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pubmed:author |
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pubmed:copyrightInfo |
(c) 2008 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
775-80
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pubmed:meshHeading |
pubmed-meshheading:18200590-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:18200590-Chromatography, High Pressure Liquid,
pubmed-meshheading:18200590-Circular Dichroism,
pubmed-meshheading:18200590-Crystallography, X-Ray,
pubmed-meshheading:18200590-Models, Molecular,
pubmed-meshheading:18200590-Molecular Conformation,
pubmed-meshheading:18200590-Molecular Structure,
pubmed-meshheading:18200590-Pyrroles,
pubmed-meshheading:18200590-Spectrophotometry, Ultraviolet,
pubmed-meshheading:18200590-Stereoisomerism
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pubmed:year |
2008
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pubmed:articleTitle |
HPLC enantioseparation and absolute configuration of novel anti-inflammatory pyrrole derivatives.
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pubmed:affiliation |
Università La Sapienza, Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, 00185 Rome, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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