The enantiomeric separation of an anti-inflammatory drug flobufen was performed on various chiral columns in liquid chromatography and by reversed phase chromatography and by capillary electrophoresis with β€cyclodextrin as a chiral selector in the mobile phase and background electrolyte, respectivel
Resolution of Racemic Jasmonic Acid and Abscisic Acid by Chiral High Performance Liquid Chromatography
β Scribed by Robert Kramell; Gernot Schneider; Otto Miersch
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 314 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0958-0344
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β¦ Synopsis
The direct resolution of racemic jasmonic acid (JA) and abscisic acid (ABA), as the free acids, into the corresponding enantiomers by high performance liquid chromatography on a Nucleodex p-PM column is reported. The resolution factors (R,,,=1.38; R,,,,=1.65) were such that the method could be applied to the separation of these racemates on a preparative scale. The racemates of methyl jasmonate and its 12-hydroxyderivative could be resolved as their respective methyl esters. The pure isomers obtained were characterized using circular dichroism and optical rotatory dispersion.
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Figure 1. Reaction of D/L-amino acids with R(Γ)-DBD-PyNCS.
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