Issue 13, 1969

Reactive intermediates, part IX. An attempted synthesis of phenanthrocyclopropenone

Abstract

The dehydrobromination of 5,7-dibromodibenzo[a,c]cycloheptadien-6-one (II) has been investigated as a possible route to phenanthrocyclopropenone (I). The products of the reactions are derivatives of 9-phenanthroic acid, but the cyclopropenone is probably not an intermediate in their formation.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 1763-1766

Reactive intermediates, part IX. An attempted synthesis of phenanthrocyclopropenone

T. L. Gilchrist and C. W. Rees, J. Chem. Soc. C, 1969, 1763 DOI: 10.1039/J39690001763

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