Synthesis and enantiomeric recognition studies of dialkyl-substituted 18-crown-6 ethers containing an acridine fluorophore unit

Júlia Kertész, Ildikó Móczár, Attila Kormos, Péter Baranyai, Miklós Kubinyi, Klára Tóth, Péter Huszthy

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Selectivity of the reported dimethyl-substituted (R,R)-1, the diisobutyl-substituted (R,R)-2 acridino-18-crown-6 ethers and the newly synthesized acridino-crown ether (S,S)-3 containing the methyl groups one carbon-carbon bond further away from the acridine unit was studied towards the enantiomers of the hydrogen perchlorate salts of α-phenylethylamine, α-(1-naphthyl)ethylamine, phenylglycine methyl ester and phenylalanine methyl ester using fluorescence.

Original languageEnglish
Pages (from-to)684-689
Number of pages6
JournalTetrahedron Asymmetry
Volume22
Issue number6
DOIs
Publication statusPublished - Mar 30 2011

    Fingerprint

ASJC Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Cite this