Preparation and application of a new doubly tethered chiral stationary phase containing NCH3 amide linkage based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Reference14 articles.
1. Characterization of liquid chromatographic chiral separation on chiral crown ether stationary phases
2. Development and Application of Crown Ether-based HPLC Chiral Stationary Phases
3. Preparation and application of HPLC chiral stationary phases based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid
4. Liquid chromatographic resolution of racemic amino acids and their derivatives on a new chiral stationary phase based on crown ether
5. Preparation and application of a new modified liquid chromatographic chiral stationary phase based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid
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1. Microsampling and enantioselective liquid chromatography coupled to mass spectrometry for chiral bioanalysis of novel psychoactive substances;Talanta;2023-05
2. Zwitterionic codeine-derived methacrylate monoliths for enantioselective capillary electrochromatography of chiral acids and chiral bases;ELECTROPHORESIS;2018-07-25
3. Liquid chromatographic resolution of proline and pipecolic acid derivatives on chiral stationary phases based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid;Journal of Separation Science;2018-01-02
4. Liquid chromatographic enantioseparations on crown ether-based chiral stationary phases;Journal of Chromatography A;2016-10
5. Development of HPLC Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and Their Applications;Chirality;2015-08-03
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