Issue 0, 1967

The conformational analysis of saturated heterocycles. Part XI. The conformation of 1-methylpiperidines from electric dipole moment studies

Abstract

Electric dipole moments of suitably substituted piperidines indicate that the methyl group in an N-methylpiperidine exists preferentially in the equatorial position.

Article information

Article type
Paper

J. Chem. Soc. B, 1967, 493-498

The conformational analysis of saturated heterocycles. Part XI. The conformation of 1-methylpiperidines from electric dipole moment studies

R. J. Bishop, L. E. Sutton, D. Dineen, R. A. Y. Jones, A. R. Katritzky and R. J. Wyatt, J. Chem. Soc. B, 1967, 493 DOI: 10.1039/J29670000493

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