Issue 14, 1969

Novel aromatic systems. Part VIII. Attempts to make a dibenzoanthrazulene

Abstract

Fluorene has been acylated with phthalic anhydride and with homophthalic anhydride; the products have been briefly studied. Reaction of fluorenoyl chloride with methyl homoveratrate gave methyl-4,5-dimethoxy-2(2-fluorenoyl)phenylacetate which was converted, in several stages, into a dihydrodibenzanthrazulene. The latter underwent oxidation to carbonyl compounds rather than dehydrogenation.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 1932-1934

Novel aromatic systems. Part VIII. Attempts to make a dibenzoanthrazulene

G. R. Proctor and J. Savage, J. Chem. Soc. C, 1969, 1932 DOI: 10.1039/J39690001932

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