Enantiomer separation and indirect chromatographic absolute configuration prediction of chiral pirinixic acid derivatives: Limitations of polysaccharide-type chiral stationary phases in comparison to chiral anion-exchangers

Michael Lämmerhofer (Korresp. Autor*in), Reinhard Pell, Marek Mahut, Martin Richter, Simone Schiesel, Heiko Zettl, Michaela Dittrich, Manfred Schubert-Zsilavecz, Wolfgang Lindner

Veröffentlichungen: Beitrag in FachzeitschriftArtikelPeer Reviewed

Abstract

Chiral ?-arylthiocarboxylic acids with different substitution patterns, representing new pirinixic acid derivatives with dual PPAR?/? agonistic activities, have been separated into enantiomers on tert-butylcarbamoylquinine and quinidine based chiral anion-exchangers and amylose tris(3,5-dimethylphenylcarbamate) coated silica on analytical and preparative scale. Absolute configurations of individual enantiomers were assigned chromatographically via elution orders on the chiral anion-exchangers and were confirmed by stereoselective syntheses via Ewans auxiliaries that have lead to enantiomeric products with known absolute configurations. The results of both methods were in full agreement. Moreover, the receptor stereoselectivity in PPAR? transactivation activities was consistent within the test set of structurally related compounds. Limited correlation (between elution order and substitution) was observed within the set of ?-arylthiocarboxylic acids on the amylose tris(3,5-dimethylphenylcarbamate) based chiral stationary phase (CSP), in particular the elution order changed with remote substitution. This clearly demonstrates the risks of chromatographic absolute configuration assignments by prediction from one structural analog to another one, especially with CSPs such as polysaccharide CSPs that are recognized for their broad applicability due to multiple binding and chiral recognition modes. It is therefore of utmost importance that such chromatographic absolute configuration predictions by extrapolation to structural analogs are combined with orthogonal methods for verification of the results.
OriginalspracheEnglisch
Seiten (von - bis)1033-1040
Seitenumfang8
FachzeitschriftJournal of Chromatography A
Jahrgang1217
Ausgabenummer7
DOIs
PublikationsstatusVeröffentlicht - 2010

ÖFOS 2012

  • 104002 Analytische Chemie

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