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Synthese des Pentacyclo-[7.3.1.14,12.02,7.06,11]tetradecans

✍ Scribed by P. V. R. Schleyer


Publisher
John Wiley and Sons
Year
1965
Tongue
English
Weight
157 KB
Volume
77
Category
Article
ISSN
0044-8249

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πŸ“œ SIMILAR VOLUMES


Pentacyclo[7.5.0.02,7.05,13.06,12]Tetrad
✍ ShΓ΄ ItΓ΄; Yutaka Fujise; M.C. Woods πŸ“‚ Article πŸ“… 1967 πŸ› Elsevier Science 🌐 French βš– 341 KB

The formation of exo-trioyolo[4.4.1.12'5 )dodecs-3,7,9-trien-11-one by the therm81 addition of tropone and oyolopentsdiene, the first example of a 6+4 cycloaddition (l), has been described recently (2). We now wish to report the synthesis of pentacyclo 17 5 o o\*,7.05\*13.06,12 . . . Jtetradeca-3,1

Syntheses and reactions of cage compound
✍ Ken-ichi Hirao; Etsuko Abe; Osamu Yonemitsu πŸ“‚ Article πŸ“… 1975 πŸ› Elsevier Science 🌐 French βš– 232 KB

Cm irradiation, cyclopentadiene dimer (3 and its enone derivatives (L,s$ are converted easily to the corresponding cage compounds, 5, 16\* 73and84 .." ,' u \_, by intramolecular cycloaddition, whereas the corresponding transformation of a six-membered analog, from cyclohexadiene dimer (9\_) to lO\_,