The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

David G. Andrews, Peter R. Ashton, Dale A. Laidler, J. Fraser Stoddart*, John B. Wolstenholme

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

The rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate.

Original languageEnglish (US)
Pages (from-to)2629-2632
Number of pages4
JournalTetrahedron Letters
Volume20
Issue number28
DOIs
StatePublished - 1979

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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