Preparation and enantiomer recognition of chiral azophenolic crown ethers having three chiral barriers on each of the homotopic faces

Koichiro Naemura*, Masaki Asada, Keiji Hirose, Yoshito Tobe

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Homochiral azophenolic crown ethers 1 and 2 having three chiral barriers, that is, the phenyl group, the methyl group, and the cyclohexane moiety on each of the homotopic faces have been prepared. The enantiomer recognition toward chiral 2-aminoethanol derivatives has been examined.

Original languageEnglish
Pages (from-to)1873-1876
Number of pages4
JournalTetrahedron: Asymmetry
Volume6
Issue number8
DOIs
StatePublished - 1 Jan 1995

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