Copper-catalyzed oxidation reactions: An alternative synthesis of 3,6-dinitroxanthone

Article abstract of DOI:10.1080/00397919308009773

Bis-(4-nitrophenyl)methane and derivatives can be oxidized to the corresponding ketones by refluxing with Cu powder in N,N-dimethylformamide (DMF). Further reaction of the 2,2'-diiodoketone, under the same conditions, leads to the title xanthone.

Full text of DOI:10.1080/00397919308009773

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Copper-Catalyzed
Oxidation Reactions: An
Alternative Synthesis of 3,6-
Dinitroxanthone
P. G. Farrell a , D. Moskowitz a & F. Terrier b
a Department of Chemistry , McGill University , 801,
Sherbrooke St. W., Montreal, Canada , H3A 2K6
b Départment de Chimie , Université de Versailles ,
45 Ave. des Etats-Unis, 78000, Versailles, France
Published online: 23 Sep 2006.
To cite this article: P. G. Farrell , D. Moskowitz & F. Terrier (1993) Copper-Catalyzed
Oxidation Reactions: An Alternative Synthesis of 3,6-Dinitroxanthone, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:2, 231-235, DOI: 10.1080/00397919308009773
To link to this article: http://dx.doi.org/10.1080/00397919308009773
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