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- W2041001056 abstract "The reaction of cyclooctatetraene oxide with ethylmagnesium bromide, phenylmagnesium bromide and t-butylmagnesium bromide was found to yield 2, 4, 6-cycloheptatrienyl-1-ethyl-, phenyl- and t-butylcarbinol respectively. The treatment of cyclooctatetraene oxide with a catalytic amount of magnesium bromide in ether afforded phenyl acetaldehyde in a 76% yield. The dehydration of the carbinols with a catalytic amount of p-toluenesulfonic acid resulted in their further rearrangement to trans-β-substituted styrenes." @default.
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- W2041001056 date "1967-01-01" @default.
- W2041001056 modified "2023-10-14" @default.
- W2041001056 title "The Reaction of Cyclooctatetraene Oxide with Grignard Reagents" @default.
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- W2041001056 doi "https://doi.org/10.1246/bcsj.40.174" @default.
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