Conclusions
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1.
1-14CH3,2,3,4-Tetramethylcyclopentadiene was synthesized and its thermal transformations were studied.
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2.
An intramolecular 1,2-shift of the methyl group is realized in the tetramethylcyclopentadiene at temperatures exceeding 400°, which leads to an equilibrium distribution of the label between the C(1)-14CH3 (or C(4)-14CH3) and the C(2)-14CH3 (or C(3)-14CH3) positions when equilibrium is reached.
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See [1] for Communication 38.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2253–2260, October, 1971.
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Mironov, V.A., Ivanov, A.P., Isagulyants, G.V. et al. Cyclic unsaturated compounds. Russ Chem Bull 20, 2128–2134 (1971). https://doi.org/10.1007/BF00851264
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DOI: https://doi.org/10.1007/BF00851264