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

DOI: 10.1039/c39940000711

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 711 - 712 (1994)

Update date:2022-08-03

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Authors:

Naemura, Koichiro

Takeuchi, Sachiko

Asada, Masaki

Hirose, Keiji

Tobe, Yoshito

et al. et al.

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Article abstract of DOI:10.1039/c39940000711

Azophenolic crown ethers 9 and 10 of C_S 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.

Full text of DOI:10.1039/c39940000711

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