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Molecular design by cycloaddition reactions. 34. Cycloaddition reactions of 1,4-[(tert-butyloxycarbonyl)imino]-1,4-dihydronaphthalene

✍ Scribed by Sasaki, Tadashi; Manabe, Takashi; Nishida, Sumio

Book ID
126210619
Publisher
American Chemical Society
Year
1980
Tongue
English
Weight
528 KB
Volume
45
Category
Article
ISSN
0022-3263

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Cycloaddition Reaction of 1,4-Dihydronaphthalene 1,4-Epoxide with Cyclooctatetraene: Cope Rearrangement in an Adduct
✍ Abdullah Menzek; Latif Kelebekli; Aliye Altundaş; Ertan Şahin; Fatoş Polat 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 German ⚖ 369 KB

## Abstract The reaction of 1,4‐dihydro‐1,4‐epoxynaphthalene with cyclooctatetraene at 130±5° for 14 days gave the four products 2a,3,3a,4,9,9a,10,10a‐octahydro‐4,9‐epoxy‐3,10‐ethenocyclobuta[__b__]anthracene (**13**), 25‐oxanonacyclo[10.10.2.2^5,9^.1^14,21^.0^2,11^.0^3,10^.0^4,6^.0^13,22^.0^15,20^