**Photolysis of Conjugated Epoxy‐dienes** Direct and sensitized excitation of the (__E__)‐β‐ionylidene‐epoxides **1** and **4** leads to different types of isomerizations. Thus photocycloelimination to the cyclopropene‐ketones **2** and **6** is only achieved by ^1^(π, π\*)‐excitation (λ=254 nm), w
✦ LIBER ✦
Photochemische Reaktionen. 89. Mitteilung [1]. Zur Photochemie konjugierter Epoxy-diene I. Versuche mit (E),β-Jonyliden-epoxiden
✍ Scribed by Alex Peter Alder; Hans Richard Wolf; Oskar Jeger
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- German
- Weight
- 469 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Photolysis of conjugated epoxy‐dienes
UV.‐irradiation (λ = 254 nm) of (E),β‐ionylidene‐epoxide (3) in n‐pentane gives the isomeric cyclopropene‐ketone 7 (90%) in a hitherto unreported type of photoreaction. The methylsubstituted (E),β‐ionylidene‐epoxide 6, however, undergoes (E/Z)‐photoisomerization to the (Z),β‐ionylidene‐epoxide 8 (91%).
📜 SIMILAR VOLUMES
Photochemische Reaktionen. 97 Mitteilung
✍
Alex Peter Alder; Hans Richard Wolf; Oskar Jeger
📂
Article
📅
1978
🏛
John Wiley and Sons
🌐
German
⚖ 923 KB