Formation and structural features of novel cage compounds with a pentacyclo[6.4.0.03,7.04,11.05,10]dodecane skeleton via photolysis of [33](1,3,5)cyclophane
โ Scribed by Kumi Matohara; Chultack Lim; Mikio Yasutake; Rika Nogita; Toru Koga; Youichi Sakamoto; Teruo Shinmyozu
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 211 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Prismanes constitute a fascinating family of (CH) n polyhedra, [1] several members of which, namely, prismane, [2] cubane, [3] and pentaprismane, [4, have been successfully synthesized. Recently, attention has focused on the challenging objective of synthesizing the higher prismanes, in particular,
The photolysis of [34](1,2,3,5)cyclophane 5 in H20-saturated CH2Clz produced the novel polycyclic caged diol 6 with a pentacyclo[6.3.1.16,1ยฐ.03,7.04,1ยฐ]dodecane skeleton 4, which has abnormally elongated C--C single bonds (1.624/k). The structural features of 6 were studied using the X-ray structura