High-performance liquid chromatographic determination of enantiomeric amino acids and amino alcohols after derivatization with o-phthaldialdehyde and various chiral mercaptans
- 31 December 1986
- journal article
- research article
- Published by Elsevier in Journal of Chromatography A
- Vol. 387, 255-265
- https://doi.org/10.1016/s0021-9673(01)94529-7
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- o-Phthalaldehyde—N-acetyl-L-cysteine as a chiral derivatization reagent for liquid chromatographic optical resolution of amino acid ernantiomers and its application to conventional amino acid analysisJournal of Chromatography A, 1986
- Off-line liquid chromatographic-mass spectrometric studies of fluorescent β-aminothiol-o-phthalaldehyde derivativesJournal of Chromatography A, 1985
- Liquid chromatographic separation of enantiomeric alkanolamines via diastereomeric tartaric acid monoestersJournal of Chromatography A, 1984
- Synthesis and liquid chromatographic evaluation of some chiral derivatizing agents for resolution of amine enantiomersAnalytical Chemistry, 1984
- High-performance liquid chromatographic resolution of enantiomers of 1-phenyl-2-aminopropanes (amphetamines) with four chiral reagentsJournal of Chromatography B: Biomedical Sciences and Applications, 1984
- Optical resolution of amino acid enantiomers by high-performance liquid chromatographyJournal of Chromatography A, 1984
- Resolution of amino acid enantiomers by high-performance liquid chromatography using automated pre-column derivatisation with a chiral reagentJournal of Chromatography A, 1984
- SMS 201–995: A very potent and selective octapeptide analogue of somatostatin with prolonged actionLife Sciences, 1982
- Resolution of enantiomers of norepinephrine and epinephrine by reversed-phase high-performance liquid chromatographyJournal of Chromatography A, 1981
- Quantitative determination of D- and L-amino acids by reaction with tert-butyloxycarbonyl-L-leucine N-hydroxysuccinimide ester and chromatographic separation as L,D and L,L dipeptidesAnalytical Chemistry, 1978