Issue 13, 1974

Dianions of β-keto-sulphoxides. A new general synthesis of vinyl ketones

Abstract

The dianion of the β-keto-sulphoxide (1) can be alkylated exclusively on the γ-carbon atom with a variety of alkyl halides; the resultant α-phenylsulphinyl ketones (3) undergo ready elimination of benzenesulphenic acid providing a new general route to alkyl vinyl ketones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 497-498

Dianions of β-keto-sulphoxides. A new general synthesis of vinyl ketones

P. A. Grieco, D. Boxler and C. S. Pogonowski, J. Chem. Soc., Chem. Commun., 1974, 497 DOI: 10.1039/C39740000497

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