The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces
Abstract
Azophenolic crown ethers 9 and 10 of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.