Asymmetric synthesis of chiral α-ferrocenylalkylamines and their use in the preparation of chiral redox-active receptors

P Laurent, H Miyaji, SR Collinson, I Prokes, CJ Moody, JHR Tucker, Alexandra Martha Zoya Slawin

Research output: Other contribution

43 Citations (Scopus)

Abstract

[GRAPHICS]

A new strategy for the asymmetric synthesis of chiral primary alpha-ferrocenylalkylamines has been utilized to generate homochiral redox-active receptors that bind chiral carboxylate anions with moderate enantioselectivity and undergo a redox response to complexation.

Original languageEnglish
Volume4
DOIs
Publication statusPublished - 14 Nov 2002

Keywords

  • ORGANOMETALLIC REAGENTS
  • ENANTIOSELECTIVE SYNTHESIS
  • MOLECULAR RECOGNITION
  • ORGANOLITHIUM COMPOUNDS
  • OXIME ETHERS
  • AMINO-ACIDS
  • 1,2-ADDITION
  • 1-FERROCENYLALKYLAMINES
  • DERIVATIVES
  • THIOUREA

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