## Abstract The two novel tricyclic C~10~H~16~ compounds __anti__‐ and __syn__‐tricyclo [4.2.1.1^2,5^]‐ decane (**16** and **17**, respectively) were synthesized starting either from the photodimer **2** (__anti__) or the two cycloaddition products **8** (__anti__) and **9** (__syn__).
Tricyclo[4.2.2.22,5] dodecane and Tricyclo [4.2.2.12,5]undecane. Preliminary communication
✍ Scribed by Beat Ernst; Camille Ganter
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- German
- Weight
- 159 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A synthesis of tricyclo [4.2.2.2^2,5^]dodecane (19), a novel tricyclic C~12~H~20~ compound, is described. The key intermediate ketone 13 was prepared either from the C~10~‐photodimer 1 of cyclopentadienone or the C~11~‐cycloaddition products 11 and 12. 13 was also transformed to tricyclo [4.2.2.1^2,5^]undecane (8).
📜 SIMILAR VOLUMES
Regioselective generation of the C(2)-carbocation a of tricyc10[4.2.2.0',~]decane (1) by treatment of both corresponding epimeric alcohols 5 and 6 with BF, and trapping the rearranged tricy~lo[S.3.0.O~~~]decan-7-yl carhocation b with Et,SiH as hydride-ion donor (ionic hydrogenation) gives the corres
## Abstract The ^13^C NMR spectra of tricyclo[4.2.1.0^2,5^]nonanes and tetracyclo[5.4.1.0^2,6^.0^8,11^]dodecanes and their dimethyl derivatives were measured to demonstrate the four‐membered ring annelation effects on the bicyclo[2.2.1]heptane skeleton, and the steric δ‐__syn__ effects of the methy