Issue 24, 1978

Substitution of allylic sulphides of benzothiazole-2-thiol with organomagnesium compounds in the presence of copper(I) iodide. A regioselective synthesis of olefins

Abstract

Primary allylic sulphides of benzothiazole-2-thiol react with butylmagnesium bromide in the presence of copper(I) iodide to yield, depending on the solvent, olefins with or without allylic rearrangement.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 1085-1086

Substitution of allylic sulphides of benzothiazole-2-thiol with organomagnesium compounds in the presence of copper(I) iodide. A regioselective synthesis of olefins

P. Barsanti, V. Calò, L. Lopez, G. Marchese, F. Naso and G. Pesce, J. Chem. Soc., Chem. Commun., 1978, 1085 DOI: 10.1039/C39780001085

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