A chiral stationary phase which affords unusually high levels of enantioselectivity

Abstract

Abstract A chiral stationary phase (CSP) derived from N ‐(1‐naphthyl) leucine has been prepared. This CSP is conceptually similar to the CSP derived from N ‐(2‐naphthyl)alanine and was expected to separate the enantiomers of the same clientele of analytes as does the latter. The magnitudes of the separation factors observed on the two CSPs may differ markedly for a given analyte, the new CSP often affording much greater enantioselectivity.