Investigation of the metabolism of 3, 4, 9, 10-dibenzpyrene
E ÜNSEREN, LF FIESER
Index: Uenseren,E.; Fieser,L.F. Journal of Organic Chemistry, 1962 , vol. 27, p. 1386 - 1389
Full Text: HTML
Citation Number: 16
Abstract
In 3, 4, 9, 10-dibenzpyrene the 5-and 8-positions are identical and thus should both possess high reactivity. In accordance with expectations, we found that the hydrocarbon is oxidized to the 5, 8-quinone I1 by either chromic acid in acetic acid or selenium dioxide in nitrobenzene. The product of reaction with lead tetraacetate was shown to be the 5, 8-diacetoxy derivative VI by the preparation of an identical product by reductive acetylation of the quinone I1 and ...
Related Articles:
[Cremonesi, Paolo; Hietbrink, Bruce; Rogan, Eleanor G.; Cavalieri, Ercole L. Journal of Organic Chemistry, 1992 , vol. 57, # 12 p. 3309 - 3312]
[Tilak et al. Tetrahedron, 1958 , vol. 3, p. 62,67]