Chiral Stationary Phases for High Performance Liquid Chromatographic Separation of Enantiomers: A Mini-Review
- 1 September 1984
- journal article
- research article
- Published by Taylor & Francis in Journal of Liquid Chromatography
- Vol. 7 (sup002) , 353-376
- https://doi.org/10.1080/01483918408073942
Abstract
There has been a proliferation of papers on the use of chiral stationary phases (CSP's) to separate optical isomers in high performance liquid chromatography. The chemistry, mechanism and stability of these CSP's can vary widely. Furthermore, the applicability, availability and cost of a CSP can mean the difference between its being of passing academic interest as opposed to a technique that could have a significant impact on science and technology. Six different classes of chiral stationary phases are examined and discussed including the new chiral cyclodextrin bonded phases. The separation mechanism, strengths and limitations of the CSP's are also considered whenever such information is available.Keywords
This publication has 51 references indexed in Scilit:
- Novel packing material for optical resolution: (+)-poly(triphenylmethyl methacrylate) coated on macroporous silica gelJournal of the American Chemical Society, 1981
- CHROMATOGRAPHIC RESOLUTION OF ENANTIOMERS HAVING AROMATIC GROUP BY OPTICALLY ACTIVE POLY(TRIPHENYLMETHYL METHACRYLATE)Chemistry Letters, 1981
- A widely useful chiral stationary phase for the high-performance liquid chromatography separation of enantiomersJournal of the American Chemical Society, 1981
- Chiral recognition by small biological molecules. Resolution of helicenes on silica gel coated with riboflavinJournal of the American Chemical Society, 1980
- Host-guest complexation. 22. Reciprocal chiral recognition between amino acids and dilocular systemsJournal of the American Chemical Society, 1980
- Chromatographic Resolution of Racemates. New analytical methods (17)Angewandte Chemie International Edition in English, 1980
- Separation of D and L Amino Acids by Liquid Chromatography: Use of Chiral EluantsScience, 1979
- Isomeric inversion of ibuprofen (r)‐enantiomer in humansJournal of Pharmaceutical Sciences, 1976
- A NEW REAGENT FOR RESOLUTION BY COMPLEX FORMATION; THE RESOLUTION OF PHENANTHRO-[3,4-c]PHENANTHRENE1Journal of the American Chemical Society, 1955
- 756. The optical resolution of aromatic amino-acids on paper chromatogramsJournal of the Chemical Society, 1952