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Issue 21, 1974
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Constitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes

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.

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Article type: Paper
DOI: 10.1039/C3974000863B
Citation: J. Chem. Soc., Chem. Commun., 1974,0, 863b-864
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    Constitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes

    I. J. Burden and J. F. Stoddart, J. Chem. Soc., Chem. Commun., 1974, 0, 863b
    DOI: 10.1039/C3974000863B

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