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

Koichiro Naemura*, Sachiko Takeuchi, Masaki Asada, Keiji Hirose, Yoshito Tobe, Takahiro Kaneda, Yoshiteru Sakata

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

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.

Original languageEnglish
Pages (from-to)711-712
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number6
DOIs
StatePublished - 1 Dec 1994

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