## Abstract The separation of racemic paroxol, a key precursor of __trans__‐(−)‐paroxetine, on Chiralpak AD‐H, an amylose‐based chiral stationary phase, by supercritical fluid chromatography was studied. Pulse experiments were investigated using supercritical carbon dioxide modified with methanol (
Chiral resolution of some antimalarial agents by sub- and supercritical fluid chromatography on an (S)-naphthylurea stationary phase
✍ Scribed by Gilles Peytavin; Dr. Françlois Gimenez; Brigitte Genissel; Catherine Gillotin; Arlette Baillet; Irving W. Wainer; Robert Farinotti
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 540 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Fast resolutions of racemic compounds (sulfoxides, amino alcohols, and α‐methylarylacetic acids derivatives) were achieved on a chiral microbore column using carbon dioxide and a polar methanol/dioxane modifier. The stationary phase used in this study contains the 3,5‐dinitrobenzoyl der
Enantiomeric separation of a variety of drugs and related compounds was achieved on an (S)-naphthylethylcarbamoylated-p-cyclodextrin (SNEC-CD) chiral stationary phase (CSP) using sub-and supercritical fluid chromatography (SFC). Compounds previously resolved on native or derivatized cyclodextrin CSP
Enantiomeric separation of chiral pesticides by high-performance liquid chromatography on an amylose tris-(S)-1-phenylethylcarbamate chiral stationary phase Amylose tris-(S)-1-phenylethylcarbamate chiral stationary phase (CSP) was prepared. The direct enantiomeric separation of chiral pesticides on