Issue 22, 1970

Formation of derivatives of cyclopropane by an oxidative cyclisation using nickel peroxide

Abstract

Treatment of ethyl cyanoacetate and three N-disubstituted derivatives of cyanoacetamide with nickel peroxide gives dimeric and/or trimeric products, the latter being derivatives of cyclopropane.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1574-1575

Formation of derivatives of cyclopropane by an oxidative cyclisation using nickel peroxide

B. T. Golding and D. R. Hall, J. Chem. Soc. D, 1970, 1574 DOI: 10.1039/C29700001574

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