E. Fogassy et D. Kozma, NONCONVENTIONAL AGENTS FOR OPTICAL RESOLUTIONS, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 276, 1996, pp. 37-45
In this paper we demonstrate the use of chiral drugs and intermediates
as resolving agents on 13 examples from our practice. In 11 cases of
13, the configuration of the enantiomers in the precipitated salt is o
pposite, which support the assumption that the formation of a ''quasi
racemate'' type diastereoisomeric salt may be preffered, when the race
mate and the resolving agent are structurally similar or at least ther
e is no significant difference between their molecular weight.