Effects of structural changes on chiral selectivity in molecular complexation

Abstract
Seven macrocyclic ethers containing 2,2′-substituted-1,1′-binaphthyl units as chiral barriers connected through different combinations of OCH2CH2OCH2-CH2O, O[CH2]5O, m-C6H4(CH2O)2 and 2,6-C5H3N(CH2O)2(substituted pyridyl) units complex differently with the enantiomers of the hexafluorophosphate salts of racemic methyl phenylglycinate and methyl valinate.

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