Issue 6, 1994

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 711-712

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

K. Naemura, S. Takeuchi, M. Asada, K. Hirose, Y. Tobe, T. Kaneda and Y. Sakata, J. Chem. Soc., Chem. Commun., 1994, 711 DOI: 10.1039/C39940000711

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