Issue 18, 1973

The apparent [2,3] sigmatropic rearrangements of acetylenic ammonium ylides

Abstract

The rearrangement reactions of acetylenic ammonium ylides are not inhibited by the steric requirements of the bicyclic systems of (7a) and (10a); accordingly a non-concerted mechanism analogous to (1)→(2)→(3) is proposed for these reactions, rather than the [2,3] concerted sigmatropic mechanism.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 657-658

The apparent [2,3] sigmatropic rearrangements of acetylenic ammonium ylides

W. D. Ollis, I. O. Sutherland and Y. Thebtaranonth, J. Chem. Soc., Chem. Commun., 1973, 657 DOI: 10.1039/C39730000657

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