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- W2023651449 abstract "The product formed from cyclopentadiene and the cyclo-octatetraene dimer 5a has been shown to possess structure 6a, probably resulting from Cope rearrangement of an initial adduct 4a. The reaction of tetraphenylcyclopentadienone with 1 - methoxybuta - 1,3 - diene yields a mixture of the exo-adduct 14 and the rearranged endo-adduct 13 Rearrangement of the norbornenone derivative 27 gives the Cope product 29 Treatment of the 4,5-fused 2,3,4,5-tetrachlorocyclopent-2-enones 29,40 and 41 with powdered sodium hydroxide in tetrahydrofuran results in ring-cleaveage with the formation of 2,3,5-trichlorobuta-2,4-dienoic acid derivatives, 36, 43 and 44 respectively." @default.
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- W2023651449 date "1977-01-01" @default.
- W2023651449 modified "2023-10-17" @default.
- W2023651449 title "Cope rearrangements of diels-alder adducts containing norbornene and norbornenone systems" @default.
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- W2023651449 doi "https://doi.org/10.1016/0040-4020(77)88017-4" @default.
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