High-performance liquid chromatographic separation of β-amino alcohols II. Separation of trans-2-(dialkylamino)cyclohexanols on an amylose-based chiral stationary phase
✍ Scribed by L.W. Nicholson; C.D. Pfeiffer; C.T. Goralski; B. Singaram
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 480 KB
- Volume
- 719
- Category
- Article
- ISSN
- 1873-3778
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
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
Penicillamine enantiomers derivatized with N-[4-(6-dimethylamino-2-benzofuranyl)phenyl]maleimide (DBPM) were separated and determined by high-performance liquid chromatography. A fluorogenic reagent, DBPM easily reacted with 1)-or L-penicillamine to give each two kinds of strong fluorescent derivati
## Abstract Direct HPLC separation of stereoisomers of three novel 5‐methyl‐2‐(alkylthio)‐6‐(2,6‐difluorophenylalkyl)‐3,4‐dihydropyrimidin‐4(3__H__)‐ones endowed with antiviral and potential antiproliferative and morphological differentiation activity against melanoma cells was performed by using t