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
(+)- 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.