Preparation of an O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine-silica hybrid monolithic column for the enantioseparation of amino acids by nano-liquid chromatography
Author:
Funder
Ministry of Economy and Competitiveness
Comunidad of Madrid
European funding from FEDER program
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference28 articles.
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3. Chiral separation of acidic compounds using an O-9-(tert-butylcarbamoyl) quinidine functionalized monolith in micro-liquid chromatography;Wang;J. Chromatogr. A,2016
4. Enantioseparation of N-derivatized amino acids by micro-liquid chromatography using carbamoylated quinidine functionalized monolithic stationary phase;Wang;J. Chromatogr. A,2014
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1. Review of recent advances in development and applications of organic‐silica hybrid monoliths;Journal of Separation Science;2023-08-15
2. Single-step fabrication of a teicoplanin functionalized organic-silica hybrid monolith for enantioseparation by nano-liquid chromatography;Journal of Chromatography Open;2021-11
3. Chiral Monolithic Silica-Based HPLC Columns for Enantiomeric Separation and Determination: Functionalization of Chiral Selector and Recognition of Selector-Selectand Interaction;Molecules;2021-08-29
4. Advancements in the preparation and application of monolithic silica columns for efficient separation in liquid chromatography;Talanta;2021-03
5. Application of porous layer open tubular capillary columns with narrow inner diameter in nanoflow-high performance liquid chromatography for N-derivatized amino acid enantiomers;CHIN J CHROMATOGR;2020
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