Abstract
Capillary electrophoresis was successfully applied for separation of the enantiomers of N-benzyloxycarbonyl-α-aminophosphonic and α-aminophosphinic acids as well as their ethyl and phenyl monoesters with the use of a range of commercially available cyclodextrins (α, β and hydroxypropyl-γ-cyclodextrins) as chiral selectors. The dependence of effectiveness of separation on type and concentration of these chiral selectors as well as on pH of background electrolyte was examined in some detail.
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