Photochemistry of 2-Alkylaminophenoxaz-3-ones. 1 I
β Scribed by Levine, Samuel G.; Wani, M. C.
- Book ID
- 126334396
- Publisher
- American Chemical Society
- Year
- 1965
- Tongue
- English
- Weight
- 792 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
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## Abstract On ultraviolet irradiation in toluene, cyclopentβ2βenβone (**1a**) and 3βmethylcyclopentβ2βenβone (**1b**) undergo dimerisation (β **3a, b, 4b**), whereas 3β__t__βbutylβcyclopentβ2βenβone (**1e**) and the bicyclo [3.2.1]octenone **2a** only react with the solvent (β **5eβ7e, 8β10**). Th
The photochemistry of 3,5-cycloheptadienones is unusually varied. 1 By contrast, however, the photochemistry of 2H-azepin-2-ones, the nitrogen-hetero analogues of 3,5-cycloheptadienones, has been suggested to be much more simple.