## Abstract Amylopectin‐__tris__(phenylcarbamate) was synthesized and coated to aminopropylsilica to prepare chiral stationary phase. The chiral separations of fungicide enantiomers were performed by the CSP using high‐performance liquid chromatography. Mobile phase was __n__‐hexane and isopropanol
Separation of racemiccloso-3,3-(η3,2-norbornadienyl)rhodacarboranes into enantiomers by HPLC on chiral stationary phasesinto enantiomers by HPLC on chiral stationary phases
✍ Scribed by M. M. Il'in; T. V. Zinevich; I. V. Pisareva; I. T. Chizhevsky; V. A. Davankov
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 156 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1573-9171
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The direct separation of -aminoester enantiomers by HPLC on synthetic chiral stationary phases based on aacidic derivative of trans 1,2-diaminocyclohexane as selector is described. The application of different columns containing the stationary phase with opposite configurations and in the racemic f
Three fungicidal triazolyl alcohols (triadimenol, hexaconazole, and cis/ trans-1-4-chlorophenyl-2-1H-1,2,4-triazol-1-yl-cycloheptanol) were completely separated into enantiomers by chiral HPLC using polysaccharide-based chiral stationary phases. A better separation was achieved on cellulose and amyl