Issue 7, 1971

Keten intermediates in the uncatalysed alcoholysis of β-keto-esters and related compounds

Abstract

Uncatalysed alcoholysis of alkyl acetoacetates and malonates occurs via a unimolecular dissociative mechanism involving concerted elimination of alcohol with resultant formation of substituted ketens as reactive intermediates.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 355-356

Keten intermediates in the uncatalysed alcoholysis of β-keto-esters and related compounds

D. S. Campbell and C. W. Lawrie, J. Chem. Soc. D, 1971, 355 DOI: 10.1039/C29710000355

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