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Photoaddition of alkenes to N-methyl-1,8-naphthalimide in methanol. Evidence for the mechanism of the formation of the tetracyclic adducts

✍ Scribed by Somich, Cathleen; Mazzocchi, Paul H.; Ammon, Herman L.

Book ID
126805881
Publisher
American Chemical Society
Year
1987
Tongue
English
Weight
782 KB
Volume
52
Category
Article
ISSN
0022-3263

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πŸ“œ SIMILAR VOLUMES

Novel photoaddition of Ξ±-methylstyrene t
Novel photoaddition of Ξ±-methylstyrene to N-methyl-1,8-naphthalimide in methanol. Formation of a tetracyclic adduct.
✍ Paul H. Mazzocchi; Cathleen Somich; Herman Ammon πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 149 KB

Photolysis of 1,8-naphthalimide and a-methylstyrene in methanol results in the formation of a novel tetracyclic product via initial electron transfer. The photochemistry of N-methylphthalimide in the presence of amethylstyrene is characterized by the formation of two products in methanol solution.