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Strategy for the chiral separation of non-acidic pharmaceuticals using capillary electrochromatography

✍ Scribed by Debby Mangelings; Jérôme Discry; Mohamed Maftouh; D. Luc Massart; Yvan Vander Heyden

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
167 KB
Volume
26
Category
Article
ISSN
0173-0835

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Updating a chiral separation strategy fo
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## Abstract A generic strategy for the chiral separation of non‐acidic pharmaceuticals was updated to complete an approach defined earlier. The selected chiral stationary phases are all polysaccharide selectors, chlorinated, and non‐chlorinated, namely Lux^®^ Amylose 2, Chiralcel^®^ OD‐RH, Lux^®^ C

Role of the charge in continuous beds in
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## Abstract This paper deals with the chiral separation of hydroxy acids using diallyl‐dimethylammonium chloride as a positive charge‐providing agent in the continuous bed. The chiral continuous bed was prepared by __in situ__ copolymerization of monomers, including an L‐4‐hydroxyproline derivative