Separation of the enantiomers of the 3,5-dinitrobenzamide derivatives of α-amino phosphonates on four chiral stationary phases
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference18 articles.
1. 1-Aminoalkylphosphonous acids. Part 1. Isosteres of the protein amino acids
2. Phosphoranaloge von Aminosäuren III1. Synthese optisch aktiver 1-Aminoalkylphosphonsäuren der (S)- und (R)-Reihe mit Hilfe von (-)-Ephedrin als Auxiliar
3. Chromatographic assignment of the configuration of 1-aminoalkane-phosphonic acids
4. OPTICALLY ACTIVE 1-AMINOALKYLPHOSPHONIC ACIDS
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2. Phosphopeptidomimetic substance libraries from multicomponent reaction: Enantioseparation on quinidine carbamate stationary phase;Journal of Chromatography A;2013-10
3. Direct high-performance liquid chromatographic enantioseparation of free α-, β- and γ-aminophosphonic acids employing cinchona-based chiral zwitterionic ion exchangers;Analytical and Bioanalytical Chemistry;2013-06-09
4. Small Molecules as Chromatographic Tools for HPLC Enantiomeric Resolution: Pirkle-Type Chiral Stationary Phases Evolution;Chromatographia;2013-05-09
5. Investigation of Chiral Self-Recognition of π-Acidic 3,5-Dinitrobenzoylleucine Derivatives;Bulletin of the Korean Chemical Society;2011-12-20
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