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Volumn 871, Issue 1-2, 2000, Pages 115-126
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Application of (1S,2S)- and (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2- propylisothiocyanate to the indirect enantioseparation of racemic proteinogenic amino acids
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Author keywords
Amino acids; Derivatization, LC; Diacetoxynitrophenylpropylisothiocyanate; Enantiomer separation
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Indexed keywords
1,3 DIACETOXY 1 (4 NITROPHENYL) 2 PROPYLISOTHIOCYANIC ACID;
AMINO ACID;
ISOTHIOCYANIC ACID DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL STRUCTURE;
CHIRALITY;
CHROMATOGRAPHY;
DERIVATIZATION;
DRUG SYNTHESIS;
ENANTIOMER;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
PRIORITY JOURNAL;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
AMINO ACIDS;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
HYDROGEN-ION CONCENTRATION;
INDICATORS AND REAGENTS;
ISOTHIOCYANATES;
KINETICS;
MAGNETIC RESONANCE SPECTROSCOPY;
STEREOISOMERISM;
TEMPERATURE;
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EID: 0033953604
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/S0021-9673(99)01090-0 Document Type: Article |
Times cited : (32)
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References (15)
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