The photosensitized rearrangement of benzobicyclo[2.2.2]octadienones
โ Scribed by Harold Hart; Roger K. Murray Jr.
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 170 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
While the most common photochemical transformation of medium-sized monocyclic S,y-unsaturated ketones involves a 1,3-acyl shift and migration of the allylic double bond,' 3-cyclohexenones such as t have been observed3 to photochemically rearrange with 1,2-acyl migration, to yield conjugated cyclopropyl ketones (2). The multiplicity of this photorearrangement has ?.
๐ SIMILAR VOLUMES
MILLER and Stiles reported the synthesis of banzobicyclo(2.2.2)octatriene (l), which is an interesting compound in view of the benzohomolog of barrelena (21, in the latest issue of the Journal of the American Chemical Society. Independently, we also had synthesized the above-mentioned compound from
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