Abstract Eight peptoid chiral stationary phases (CSPs) terminated with N′-substituted phenyl-L-proline or L-leucine amide were prepared and evaluated under normal phase mode. With 59 racemic analytes, we compared the enantiomeric separations on CSPs terminated with p-methylphenyl, p-chlorophenyl and unsubstituted phenyl. For short peptoid selectors containing only one SN-(1-phenylethyl) glycine (Nspe) unit, the terminal p- ...
