Mixture with equal amounts of left- and right-handed enantiomers of a chiral molecule.
1
Compound 14 was obtained as a racemate.
2
Extensive behavioral characterization has been carried out using the racemate, but limited investigation has been performed with the individual isomers.
3
The series of compounds was employed as the racemates.
4
On many occasions, the chiral pores of the MOPMs have been utilized in order to achieve separation of enantiomers from racemates.
5
The pharmacological activity of the two racemates and the two enantiomeric pairs was tested in vitro on a strip of rabbit descending thoracic aorta.
6
New compounds belonging to the class of arylethanolamines bearing one or two stereogenic centres were prepared in good yields as racemates and optically active forms.