Chiral recognition by configurationally chiral cryptands

W. David Curtis, Dale A. Laidler, J. Fraser Stoddart*, Graham H. Jones

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

1,1′,4,4′-Tetra-O-triphenylmethyl-2,2′:3,3′-bis-O- oxydiethylenedi-L-threitol [LL-(3)] and 1,2:1′,2′:5,6:5′, 6′-tetra-O-isopropylidene-3,3′:4,4′- bis-O-oxydiethylenedi-D- mannitol [DD-(4)] exhibit enantiomeric differentiation in complexation equilibria towards (±)-(RS)-α-phenylethylammonium hexafluorophosphate.

Original languageEnglish (US)
Pages (from-to)835-837
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number20
DOIs
StatePublished - 1975

ASJC Scopus subject areas

  • Molecular Medicine

Fingerprint

Dive into the research topics of 'Chiral recognition by configurationally chiral cryptands'. Together they form a unique fingerprint.

Cite this