Separation of the enantiomers of the 3,5-dinitrobenzamide derivatives of α-amino phosphonates on four chiral stationary phases
✍ Scribed by William H. Pirkle; J.Andrew Burke
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 765 KB
- Volume
- 598
- Category
- Article
- ISSN
- 1873-3778
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A liquid chromatographic ligand exchange chiral stationary phase (CSP) derived from (S)-leucinol was applied in the separation of the enantiomers of 12 beta-amino acids. The resolution was quite successful especially for the enantiomers of beta-amino acids containing aromatic functional group in the
## 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
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.