Ahuja, 1991 - Google Patents
Chiral separations: An overviewAhuja, 1991
View PDF- Document ID
- 6461928207727736432
- Author
- Ahuja S
- Publication year
External Links
Snippet
Optically active compounds have attracted great attention because living systems are chiral. Proteins, nucleic acids, and polysaccharides possess chiral characteristic structures that are related closely to their functions. Because of chirality, living organisms usually show different …
- 150000001875 compounds 0 abstract description 33
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Armstrong et al. | Enantiomeric separations in chromatography | |
| Gübitz | Separation of drug enantiomers by HPLC using chiral stationary phases—a selective review | |
| Davankov | Analytical chiral separation methods (IUPAC Recommendations 1997) | |
| Lam et al. | Reversed-phase high-performance liquid chromatographic resolution of d-and d-Dns-amino acids by mixed chelate complexation. | |
| Ikai et al. | Immobilized-type chiral packing materials for HPLC based on polysaccharide derivatives | |
| Pirkle et al. | Chiral Stationary Phases for the Direct LC Separation of | |
| Płotka et al. | Common methods for the chiral determination of amphetamine and related compounds I. Gas, liquid and thin-layer chromatography | |
| Mehta | Direct separation of drug enantiomers by high-performance liquid chromatography with chiral stationary phases | |
| Arai | Chiral separation of pharmaceuticals possessing a carboxy moiety | |
| Ahuja | Chiral separations: An overview | |
| Brash et al. | [22] High-performance liquid chromatography for chiral analysis of eicosanoids | |
| US4290893A (en) | Separation of amino acids by liquid chromatography using chiral eluants | |
| Ekelund et al. | Chiral separations of β-blocking drug substances using chiral stationary phases | |
| Florance et al. | High-performance liquid chromatographic separation of peptide and amino acid stereoisomers | |
| Martens et al. | Direct thin layer chromatographic enantioseparation of active pharmaceutical ingredients via non-covalent diastereomers | |
| Czerwenka et al. | Micro-HPLC and standard-size HPLC for the separation of peptide stereoisomers employing an ion-exchange principle | |
| Calleri et al. | Evaluation of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxyalkanoic acids, isosteric analogs and 2-arylpropionic acids | |
| Krstulovic | Chiral stationary phases for the liquid chromatographic separation of pharmaceuticals | |
| Caude et al. | Chiral stationary phases derived from tyrosine | |
| Karnes et al. | Enantiomeric resolution of drug compounds by liquid chromatography | |
| Duncan | Chiral separations: a comparison of HPLC and TLC | |
| Zief et al. | Selection of the mobile phase for enantiomeric resolution via chiral stationary phase columns | |
| Aboul-enein et al. | Direct HPLC resolution of racemic nomifensine hydrogen maleate using a chiral beta-cyclodextrin-bonded stationary phase | |
| Zhu et al. | Novel chiral stationary phases based on 3, 5‐dimethyl phenylcarbamoylated β‐cyclodextrin combining cinchona alkaloid moiety | |
| Olsen et al. | Chiral separations of β-blocking drug substances using derivatization with chiral reagents and normal-phase high-performance liquid chromatography |