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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

โœ 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

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๐Ÿ“œ SIMILAR VOLUMES


Formation of a Novel Cage Compound with
โœ Chultack Lim; Mikio Yasutake; Teruo Shinmyozu ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 112 KB ๐Ÿ‘ 1 views

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,

Photolysis of [34](1,2,3,5)cyclophane: f
โœ Chultack Lim; Mikio Yasutake; Teruo Shinmyozu ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 207 KB

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