All-cis-[5.5.5.5]fenestrane
β Scribed by Marcel Luyten; Prof. Dr. Reinhart Keese
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 258 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0044-8249
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π SIMILAR VOLUMES
The efficient synthesis of all-cis-[5.5.5.5]fenestrane (2) from the readily available intermediate 3 allowed the electron-diffraction analysis of 2. This structure analysis revealed long C-C bonds in the central C(C), fragment and a twist-envelope conformation for the four cyclopentane substructures
## Abstract The synthesis of (allβ__cis__)β[5.5.5.5]fenestrane (**3**) from dicyclopentadiene is reported. Key step is the Pdβcatalyzed reductive deoxygenation of an appropriately substituted cyclooctanone, which leads to transannular C,Cβbond formation.
The synthesis of tetracyclo15.4.1.0 4~12.0g~121dodecan-6-one JJ via an intramolecular photocycloadditlon, its reduction to the hydrocarbon Q, and its ring-contraction to tetracyclo-[4 4 1 03\*11.09JI . . . lundecane derivative g is described. The hydrocarbon tetracyclo13.3.1.03~g.07~glnonane ,I, kno