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Novel aromatic systems. Part VIII. Attempts to make a dibenzoanthrazulene
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39690001932
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.

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