Nitro-nitrite rearrangement and intramolecular cycloaddition in the photochemistry of nitro-olefins
β Scribed by Isao Saito; Hasaaki Takami; Teruo Matsuura
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 217 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In 1964 Chapman et al have reported a photorearrangement of a,B-unsaturated nitro-9--s olefins to a-oximino ketones. 2 Thereafter, a large number of examples of the nitro to nitrite rearrangement have been shown in the photochemistry of nitro-olefins 3 and of nitro aromatic 1058 (1971); c) 0. L.
π SIMILAR VOLUMES
Ab initio multicontlguration-based calculations have been performed on the nitro and nitrite adducts formed in the reaction between silyl radicals and nitrogen dioxide. Silyl radical binds to the nitrogen and oxygen atoms of NO1 with binding energies of about 53 and 77 kcal/mol, respectively. In mar
The photochemical behaviour of 2-methyl-5-nitro-I H-imidazoles 1 in water-containing solutions has been studied. In a first reaction step, the photorearrangement of 1 yields 2-methyl-2-imidazoline-4,5-dione-4-oximes 2. Hydrolysis of 2 and subsequent elimination of water from a supposed intermediate
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