Thin Layer Chromatography in Chiral Separations and AnalysisTeresa Kowalska, Joseph Sherma Thin layer chromatography (TLC) is well suited for performing enantioseparations for research as well as larger-scale applications. A fast, inexpensive, and versatile separation technique, there are many practical considerations that contribute to its effectiveness. Thin Layer Chromatography in Chiral Separations and Analysis is the first bo |
Contents
| 1 | |
Chapter 2 Chirality | 11 |
Chapter 3 Commercial Precoated Layers for Enantiomer Separations and Analysis | 43 |
Chapter 4 Planar Chromatographic Enantioseparations on Noncommercial CSPs | 65 |
Chapter 5 Planar Chromatography Enantioseparations on Noncommercial CCSPs | 111 |
Chapter 6 Chiral Mobile Phase Additives | 147 |
Chapter 7 An Overview of the Chiral Separation Mechanisms | 173 |
Chapter 8 Separation of Diastereoisomers by Means of TLC | 197 |
Chapter 10 Chirality of Pharmaceutical Products | 255 |
Chapter 11 Chiral Separation of βAdrenergic Antagonists | 283 |
Chapter 12 Chiral Separation of Amino Acid Enantiomers | 305 |
Chapter 13 Chiral Separation of Nonsteroidal AntiInflammatory Drugs | 323 |
Chapter 14 Determination of Components in Selected Chiral Drugs | 357 |
Chapter 15 Chiral Separations Using Marfeys Reagent | 383 |
| 409 | |
Chapter 9 Selected Bottlenecks of Densitometric Detection with Chiral Analytes | 231 |
Other editions - View all
Thin Layer Chromatography in Chiral Separations and Analysis Teresa Kowalska,Joseph Sherma Limited preview - 2007 |
Thin Layer Chromatography in Chiral Separations and Analysis Teresa Kowalska,Joseph Sherma No preview available - 2019 |
Thin Layer Chromatography in Chiral Separations and Analysis Teresa Kowalska,Joseph Sherma No preview available - 2007 |
Common terms and phrases
acetic addition agent amino acids analysis analytes application atom basic Bhushan bonded carbon cellulose centers Chem chemical chiral selector chiral separation chromatography coated column complexes compounds concentration configuration containing derivatives derivatization described detection determination diastereoisomers diastereomers direction drugs edited effect eluents enantiomeric enantiomers enantioseparation example factor Figure formation groups higher HPLC ibuprofen important impregnated increase interactions isomers Kowalska layers Lepri liquid mechanism method mixture mobile phase modified molecule natural observed obtained occur optically active organic pairs performed Planar Chromatogr planar chromatography plates polymers possible prepared present propranolol pure racemic ratio reaction reagent recognition References relative reported resolution resolved respectively retention Rf values ring sample selected separation showed shown silica gel solution solvent stationary phase stereoisomers structure studies substituents Table technique temperature
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