The tricyclic enedione, which was synthesized in the [2+2] photocycloaddition of homoquinone with alkyne, underwent a novel Lewis acid-mediated skeletal rearrangement to provide bi-, tri-and tetracyclic cage compounds, depending on the identity of the Lewis acid used. The prolonged reaction and the
β¦ LIBER β¦
Mechanism of Novel Consecutive Rearrangements of Cyclobutene-Fused Diphenylhomobenzoquinones Catalyzed by Lewis Acids
β Scribed by Koizumi, Takuya; Mochizuki, Eiko; Kokubo, Ken; Oshima, Takumi
- Book ID
- 126034936
- Publisher
- American Chemical Society
- Year
- 2004
- Tongue
- English
- Weight
- 186 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0022-3263
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