Issue 21, 1974

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 863b-864

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, 863b DOI: 10.1039/C3974000863B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements