Synthesis of new C3 symmetric amino acid- and aminoalcohol-containing chiral stationary phases and application to HPLC enantioseparations
Author:
Affiliation:
1. Department of Chemistry; Kyungpook Nat'l University; Daegu South Korea
2. Department of Chemistry; University of Texas; Arlington Texas USA
3. Department of Chemistry Education; Kyungpook Nat'l University; Daegu South Korea
Funder
Korean Foundation for Cancer Research
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.22766/fullpdf
Reference17 articles.
1. Chiral recognition using a conformationally rigid chiral stationary phase derived from α-amino-ϵ-carprolactam;Han;J Liq Chromatogr Relat Technol,2014
2. Novel carbamoyl type quinine and quinidine based chiral anion exchangers implementing alkyne-azide cycloaddition immobilization chemistry;Hettergger;J Chromatogr A,2014
3. Liquid chromatographic resolution of amino acid esters of acyclovir including racemic valacyclovir on crown ether-based chiral stationary phases;Ahn;Chirality,2015
4. Restricted access chiral stationary phase synthesized via reversible addition-fragmentation chain-transfer polymerization for direct analysis of biological samples by high performance liquid chromatography;Song;Anal Chim Acta,2014
5. Synthesis and enantioseparation behaviors of novel immobilized 3,5-dimethylphenylcarbamoylated polysaccharide chiral stationary phases;Tan;J Sep Sci,2014
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