Issue 19, 1972

Mechanism of reactions of sulphonium salts with organolithium reagents

Abstract

Labelling experiments have established that tetraphenylsulphurane is the principal intermediate in the reaction of phenyl-lithium with triphenylsulphonium tetrafluoroborate to give biphenyl and diphenyl sulphide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1079-1080

Mechanism of reactions of sulphonium salts with organolithium reagents

D. Harrington, J. Weston, J. Jacobus and K. Mislow, J. Chem. Soc., Chem. Commun., 1972, 1079 DOI: 10.1039/C39720001079

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