Derivatization with fluorogenic benzofurazan reagents of amino acid enantiomers and their separation on a pirkle column
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry
Reference11 articles.
1. Sensitive determination of enantiomers of amino acids derivatized with the fluorogenic reagent, 4-fluoro-7-nitro-2,1,3-benzoxadiazole, separated on a pirkle-type column, sumichiral OA 2500(S)
2. Fluorogenic reagents, having benzofurazan structure, in liquid chromatography
3. Separation of the enantiomers of the 3,5-dinitrobenzamide derivatives of α-amino phosphonates on four chiral stationary phases
4. New fluorogenic reagent having halogenobenzofurazan structure for thiols: 4-(aminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole
5. Fluorogenic reagent for thiols: 4-(N,N-dimethylaminosulphonyl)-7-fluoro-2,1,3-benzoxadiazole
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1. Pirkle-Type and Related Chiral Stationary Phases;Chiral Separations By Liquid Chromatography And Related Technologies;2003-06-03
2. Analytical Chemical Studies on High-Performance Recognition and Detection of Bio-molecules in Life;YAKUGAKU ZASSHI;2003
3. Fluorogenic and fluorescent labeling reagents with a benzofurazan skeleton;Biomedical Chromatography;2001
4. A study of chiral recognition for NBD-derivatives on a Pirkle-type chiral stationary phase;Biomedical Chromatography;2001
5. Preparation and evaluation of new Pirkle type chiral stationary phases with long alkyl chains for the separation of amino acid enantiomers derivatized with NBD-F;The Analyst;1998
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