From 1-phenyl-2-propylamine, selegiline hydrochloride, an anti-Parksins drug, was synthesized via N-methylation, enantiomer separation, N-alkylation and salt formation with an overall yield of 42.2%.
The enantiomer that rotates the plane to the right is referred to as the dextrorotatory.
Comparison of two derivatization methods for enantiomer profiling of methamphetamine
Monitoring precursor chemicals through enantiomer profiling of methamphetamine in urine
Determination of S,S-enantiomer in(1R,2R)-(-)-1,2-cyclohexanediamine by GC
The method and technical development of acetonation of hexabasic alcohol, and its application in the synthesis of one enantiomer of drugs were reviewed.
In response to the best conditions, the reaction rate achieved 98.5% and the enantiomer excess value achieved 100%.