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Volumn 998, Issue 1-2, 2003, Pages 73-82
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Design of chiral monochloro-s-triazine reagents for the liquid chromatographic separation of amino acid enantiomers
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Author keywords
Amino acids; Derivatization, LC; Diastereomer separation; Enantiomer separation, indirect; Monochloro s triazine reagents, chiral
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Indexed keywords
AMINO ACIDS;
CHLORINE;
ESTERS;
SYNTHESIS (CHEMICAL);
CHIRAL DERIVATIZING REAGENTS (CDR);
LIQUID CHROMATOGRAPHY;
2,4,6 TRICHLORO 1,3,5 TRIAZINE;
ALANINE DERIVATIVE;
AMIDE;
AMINO ACID;
CHLORINE;
CHLORINE DERIVATIVE;
ESTER DERIVATIVE;
LYSINE DERIVATIVE;
N (4 BUTOXY 6 CHLORO[1,3,5]TRIAZIN 2 YL)ALANINAMIDE;
N (4 CHLORO 6 METHOXY[1,3,5]TRIAZIN 2 YL)PHENYLALANINAMIDE;
N (4 CHLORO 6 METHOXY[1,3,5]TRIAZIN 2 YL)VALINAMIDE;
N (4 CHLORO 6 PHENOXY[1,3,5]TRIAZIN 2 YL)ALANINAMIDE;
N [4 CHLORO 6 (1,1,1 TRIFLUOROETHOXY)[1,3,5]TRIAZIN 2 YL]PHENYLALANINAMIDE;
N [4 CHLORO 6 (2 NITROPHENOXY)[1,3,5]TRIAZIN 2 YL]ALANINAMIDE;
N [4 CHLORO 6 (4 METHYL 7 BENZO[B] ALPHA PYRONYL)OXY[1,3,5]TRIAZIN 2 YL]ALANINAMIDE;
N [4 CHLORO 6 (4 PHENYLPHENOXY)[1,3,5]TRIAZIN 2 YL]ALANINAMIDE;
PROLINE DERIVATIVE;
REAGENT;
TRIAZINE;
TRIAZINE DERIVATIVE;
UNCLASSIFIED DRUG;
AMINO ACID SUBSTITUTION;
ATOM;
CHIRAL CHROMATOGRAPHY;
CHIRALITY;
CONFERENCE PAPER;
DERIVATIZATION;
DIASTEREOISOMER;
ENANTIOMER;
LIQUID CHROMATOGRAPHY;
MICELLAR ELECTROKINETIC CHROMATOGRAPHY;
PRIORITY JOURNAL;
STRUCTURE ACTIVITY RELATION;
SUBSTITUTION REACTION;
SYNTHESIS;
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EID: 0038054212
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/S0021-9673(03)00638-1 Document Type: Conference Paper |
Times cited : (41)
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References (21)
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