4-(6-METHOXY-2-NAPHTHYL)-2-BUTYL CHLOROFORMATE ENANTIOMERS - NEW REAGENTS FOR THE ENANTIOSPECIFIC ANALYSIS OF AMINO-COMPOUNDS IN BIOGENIC MATRICES

Citation
R. Buschges et al., 4-(6-METHOXY-2-NAPHTHYL)-2-BUTYL CHLOROFORMATE ENANTIOMERS - NEW REAGENTS FOR THE ENANTIOSPECIFIC ANALYSIS OF AMINO-COMPOUNDS IN BIOGENIC MATRICES, Journal of pharmaceutical and biomedical analysis, 15(2), 1996, pp. 201-220
Citations number
69
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
07317085
Volume
15
Issue
2
Year of publication
1996
Pages
201 - 220
Database
ISI
SICI code
0731-7085(1996)15:2<201:4CE-NR>2.0.ZU;2-O
Abstract
(+)- and (-)-4-(6-methoxy-2-naphthyl)-2-butyl chloroformate (NAB-C) we re prepared from the prochiral non-steroidal anti-inflammatory agent n abumetone with the aim of developing easily detectable chloroformate r eagents for the enantiospecific HPLC analysis of amino compounds in bi ogenic matrices on achiral stationary phases. The new reagents were te sted in the derivatization of beta-adrenoceptor antagonists and anti-a rrhythmic agents and allowed derivatization in the presence of water. (+)- and (-)-NAB-C were compared with other reagents with a 6-methoxy- 2-naphthyl moiety as a chromophore. The reagents were suitable for the analysis of nanogram amounts of, for example, metoprolol enantiomers in plasma, a prerequisite for application in pharmaco- or toxicokineti c studies.