Issue 0, 1967

Nuclear magnetic resonance study of the conformational isomerisation of tetrahydropyran

Abstract

The kinetic parameters of ring inversion of tetrahydropyran have been determined by the line-width method. The result of this investigation shows that the conformational mobility of the ring in comparison with that of cyclohexane is not sensibly affected by the oxygen atom.

Article information

Article type
Paper

J. Chem. Soc. B, 1967, 1203-1204

Nuclear magnetic resonance study of the conformational isomerisation of tetrahydropyran

G. Gatti, A. L. Segre and C. Morandi, J. Chem. Soc. B, 1967, 1203 DOI: 10.1039/J29670001203

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