Reaction of superoxide and ozonate radical-ions with 9, 10-dichloro-9, 10-diphenyldihydroanthracene
AR Forrester, V Purushotham
Index: Forrester, Alexander R.; Purushotham, Vemeshetti Tetrahedron Letters, 1987 , vol. 28, # 28 p. 3279 - 3282
Full Text: HTML
Citation Number: 2
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Reaction of (a) superoxide and (b) ozonate radical-ions with the title dichloride does not give the corresponding endo-peroxide and ozonide, respectively. A variety of products formed by nucleophilic substitution and reductive dehalogenation were isolated.
Related Articles:
Intramolecular nucleophilic addition of aryl bromides to ketones catalyzed by palladium
[Quan, Long Guo; Lamrani, Mouad; Yamamoto, Yoshinori Journal of the American Chemical Society, 2000 , vol. 122, # 19 p. 4827 - 4828]
Elucidation of the electron transfer reduction mechanism of anthracene endoperoxides
[Donkers, Robert L.; Workentin, Mark S. Journal of the American Chemical Society, 2004 , vol. 126, # 6 p. 1688 - 1698]
[Watanabe; Snieckus Journal of the American Chemical Society, 1980 , vol. 102, # 4 p. 1457 - 1460]
Photo-oxygénation d'amines aromatiques endoperoxydes d'amino-9 anthracènes
[Santamaria, Jean; Rigaudy, Jean Tetrahedron, 1980 , vol. 36, p. 2453 - 2457]
Hydroxy-and Methoxyphenylanthrones. III1
[Blicke; Warzynski Journal of the American Chemical Society, 1940 , vol. 62, p. 3191,3192]