Abstract
The chiral selectivities of N-(tert.-butylaminocarbonyl)-(S)-valylaminopropylsilica gel and (R)-1-(α-naphthyl)-ethyl-aminocarbonyl-glycylaminopropylsilica gel were studied using model compounds. The differences in the final energy values of molecular interactions between the model chiral phase and derivatized (R)-and (S)-amino acids, calculated by molecular.