Issue 9, 1981

New method for preparing βγ-unsaturated ketones: use of phenylselenoacetaldehyde

Abstract

Zinc enolates derived from ketones condense efficiently with phenylselenoacetaldehyde and the products are converted into βγ-unsaturated kmmetones by the action of methanesulphonyl chloride and triethylamine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 434-436

New method for preparing βγ-unsaturated ketones: use of phenylselenoacetaldehyde

D. L. J. Clive and C. G. Russell, J. Chem. Soc., Chem. Commun., 1981, 434 DOI: 10.1039/C39810000434

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