Issue 40, 2014

C–C bond migration in the cycloisomerization of oxygen-tethered 1,6-enynes

Abstract

A C–C bond migration event during the cycloisomerization of 1,6-enynes is described. Two different catalytic systems, iridium- or platinum-based, are able to induce this process. Alkyl migrations of larger rings and acyclic groups indicate that the reaction is not fully driven by the release of ring strain.

Graphical abstract: C–C bond migration in the cycloisomerization of oxygen-tethered 1,6-enynes

Supplementary files

Article information

Article type
Communication
Submitted
30 ruj 2013
Accepted
26 stu 2013
First published
27 stu 2013

Chem. Commun., 2014,50, 5239-5241

C–C bond migration in the cycloisomerization of oxygen-tethered 1,6-enynes

S. M. Stevenson, E. T. Newcomb and E. M. Ferreira, Chem. Commun., 2014, 50, 5239 DOI: 10.1039/C3CC47499B

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.

Social activity

Spotlight

Advertisements