Recognizing that the stereochemical structure of NMDA receptor antagonist ketamine provides valuable data about the relationship between its conformation and absolute configuration by CD-UV analysis, a method for the identification of ketamine enantiomers is proposed which avoids the need for authentic samples of the enantiomers. The ketamine enantiomers were separated by HPLC using Chiralcel OJ stationary phase. The in situ registration of CD and UV spectra, together with the application of the octant rule for cyclohexanone derivatives, makes possible the direct assignment of the eluted ketamine enantiomers
ABSTRACT: Heptakis(2,3-di-O-acetylated)-b-cyclodextrin was tested for its utilizability to check the...
This paper describes an enzymic derivatization procedure that allows accurate determination of very ...
Several optically active mandelic acid analogues were shown to allow a direct H-1-NMR determination ...
Ketamine (2-(2-chlorophenyl)-2-(methylamino)cyclohexanone) is a human and veterinary anaesthetic and...
The chiral drug ketamine has long-lasting antidepressant effects with a fast onset and is also suita...
Determining the absolute configuration of biologically active chiral substances is a current issue i...
Ketamine ((R,S-2-(2-chlorophenyl)-2-methylamino)cyclohexanone) is a phencyclidine derivative used in...
The chiral drug ketamine has long-lasting antidepressant effects with a fast onset and is also suita...
During the past several years, the frequency of discovery of new molecular entities based on γ- or δ...
The synthesis of enantiomerically pure compounds is an important objective of the organic chemistry....
Chiral metabolites of ketamine exerting rapid-onset yet sustained antidepressant effects may be mark...
To obtain enantiopure compounds, the so-called chiral high performance liquid chromatography (HPLC) ...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
CE with multiple isomer sulfated beta-CD as the chiral selector was assessed for the simultaneous an...
A direct HPLC enantioseparation of three representative compounds of a new family of potential non-p...
ABSTRACT: Heptakis(2,3-di-O-acetylated)-b-cyclodextrin was tested for its utilizability to check the...
This paper describes an enzymic derivatization procedure that allows accurate determination of very ...
Several optically active mandelic acid analogues were shown to allow a direct H-1-NMR determination ...
Ketamine (2-(2-chlorophenyl)-2-(methylamino)cyclohexanone) is a human and veterinary anaesthetic and...
The chiral drug ketamine has long-lasting antidepressant effects with a fast onset and is also suita...
Determining the absolute configuration of biologically active chiral substances is a current issue i...
Ketamine ((R,S-2-(2-chlorophenyl)-2-methylamino)cyclohexanone) is a phencyclidine derivative used in...
The chiral drug ketamine has long-lasting antidepressant effects with a fast onset and is also suita...
During the past several years, the frequency of discovery of new molecular entities based on γ- or δ...
The synthesis of enantiomerically pure compounds is an important objective of the organic chemistry....
Chiral metabolites of ketamine exerting rapid-onset yet sustained antidepressant effects may be mark...
To obtain enantiopure compounds, the so-called chiral high performance liquid chromatography (HPLC) ...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
CE with multiple isomer sulfated beta-CD as the chiral selector was assessed for the simultaneous an...
A direct HPLC enantioseparation of three representative compounds of a new family of potential non-p...
ABSTRACT: Heptakis(2,3-di-O-acetylated)-b-cyclodextrin was tested for its utilizability to check the...
This paper describes an enzymic derivatization procedure that allows accurate determination of very ...
Several optically active mandelic acid analogues were shown to allow a direct H-1-NMR determination ...