Issue 1, 1986

C–C bond formation from dimethyl ether via a radical mechanism in the presence of strong acid

Abstract

The selective radical dimerization of dimethyl ether by peroxodisulphuryl difluoride in fluorosulphuric acid, suggests that a radical intermediate for initial C–C bond formation in the conversion of methanol in the conversion of methanol into hydrocarbons is a possibility.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 6-7

C–C bond formation from dimethyl ether via a radical mechanism in the presence of strong acid

H. Choukroun, D. Brunel and A. Germain, J. Chem. Soc., Chem. Commun., 1986, 6 DOI: 10.1039/C39860000006

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