Stereospecific synthesis of the trans-anti-trans- and trans-syn-trans- isomers of dicyclohexyl-18-crown-6

J. Fraser Stoddart*, Colin M. Wheatley

*Corresponding author for this work

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

The macrocyclic polyethers, (7) and (8), have been synthesised stereospecifically from the diastereoisomeric acyclic methylene acetals, (1) and (2), obtained from (±)-cyclohexane-trans-1,2-diol; both (7) and (8) form stable complexes with metal cations.

Original languageEnglish (US)
Pages (from-to)390-391
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number10
DOIs
StatePublished - Jan 1 1974

ASJC Scopus subject areas

  • Molecular Medicine

Fingerprint Dive into the research topics of 'Stereospecific synthesis of the trans-anti-trans- and trans-syn-trans- isomers of dicyclohexyl-18-crown-6'. Together they form a unique fingerprint.

Cite this