Constitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes

Ian J. Burden, J. Fraser Stoddart*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

The equilibrium proportions of the constitutional isomers (1)-(4) and the conformational behaviour of the cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes (1a)-(4a) provide no evidence for the gauche arrangement of the vicinal oxygen substituents being a stabilising feature in these systems.

Original languageEnglish (US)
Pages (from-to)863b-864
JournalJournal of the Chemical Society, Chemical Communications
Issue number21
DOIs
StatePublished - 1974

ASJC Scopus subject areas

  • Molecular Medicine

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