## Abstract The photo‐oxidation of the title compound (**1**) is described. The isolated products are the result of a [2 + 2] oxygen addition to the olefinic double bond of the enamide.
Photochemical Reactions. IV. [1] Irradiation of 17 β-acetoxy-4-aza-androst-5-en-3-one with UV.-light
✍ Scribed by José Boix; José Gómez; Juan-Julio Bonet
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 475 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The photochemical behaviour of the title compound (7) is described. The obtained results indicate the high reactivity of the enamidic Δ^5^ double bond.
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## Abstract The irradiation of the title compound **6** with UV. light and under photosensitized oxidation conditions yields products which are characteristic of the photo‐oxidation of the enamide moiety of **6**. In contrast to the situation encountered in the case of the irradiation of its carboc
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