Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens

Chirality

Volumn 11, Issue 4, 1999, Pages 291-300

  Olšovská, Jana ^a   Flieger, Miroslav ^a   Bachechi, Fiorella ^b   Messina, Antonella ^c   Sinibaldi, Massimo ^b  

^a INSTITUTE OF MICROBIOLOGY   (Czech Republic)

^b CNR   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Chiral recognition mechanism; Ergot alkaloid based stationary phases; HPLC enantioseparation; Non steroidal anti inflammatory drugs (NSAIDs); Plasma; Semipreparative scale separation

Indexed keywords

ARYLPROPIONIC ACID DERIVATIVE; FENOPROFEN; FLOBUFEN; IBUPROFEN; NAPROXEN; SUPROFEN; TERGURIDE;

ARTICLE; CHIRALITY; CRYSTAL STRUCTURE; DRUG ISOLATION; DRUG STRUCTURE; ENANTIOMER; ISOMERISM; PRIORITY JOURNAL; X RAY ANALYSIS;

ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; BUTYRIC ACIDS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ERGOLINES; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PROPIONIC ACIDS; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0042241691     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1999)11:4<291::AID-CHIR6>3.0.CO;2-4     Document Type: Article

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