Issue 22, 1971

Electrochemical reduction of 1,4-diphosphoniacyclohexa-2,5-diene salts without accompanying cleavage

Abstract

Controlled potential electrochemical reduction of 1,4-diphosphoniacyclohexa-2,5-diene salts in aqueous ethanol provides good yields of 1,1,4,4-tetrasubstituted-1,4-diphosphoniacyclohexane dichlorides or dibromides without reductive cleavage of the ring or any external carbon–phosphorus bonds, including those of substituted benzyl groups.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1478-1479

Electrochemical reduction of 1,4-diphosphoniacyclohexa-2,5-diene salts without accompanying cleavage

J. H. Stocker, R. M. Jenevein, A. Aguiar, G. W. Prejean and N. A. Portnoy, J. Chem. Soc. D, 1971, 1478 DOI: 10.1039/C29710001478

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