Recognizing that the stereochemical structure of NMDA receptor antagonist k
etamine provides valuable data about the relationship between its conformat
ion and absolute configuration by CD-UV analysis, a method for the identifi
cation of ketamine enantiomers is proposed which avoids the need for authen
tic samples of the enantiomers. The ketamine enantiomers were separated by
HPLC using Chiralcel OJ stationary phase. The in situ registration of CD an
d UV spectra, together with the application of the octant rule for cyclohex
anone derivatives, makes possible the direct assignment of the eluted ketam
ine enantiomers. Chirality 11:741-744, 1999. (C) 1999 Wiley-Liss, Inc.