Abstract
M. G. GONIKBERG et al.1–3 have recently found that at high pressures the attack of phenyl radicals on tertiary butyl benzene yields an appreciably higher proportion of the sterically strained 2-phenyl isomer than it does at atmospheric pressure.
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References
Gonikberg, M. G., Prokhorova, N. I., and Litvin, E., Izv. Akad. Nauk. S.S.S.R. (Otd. Khim. Nauk.), No. 8, 1495 (1962).
Gonikberg, M. G., Prokhorova, N. I., and Litvin, E., Doklady Akad. Nauk. S.S.S.R., 148, 105 (1963).
Gonikberg, M. G., Zhur. Fiz. Khim., 37, 477 (1963).
Coillet, D. W., and Hamann, S. D., Trans. Farad. Soc., 57, 2231 (1961).
Olah, G. A., and Kuhn, S. J., J. Amer. Chem. Soc., 84, 3684 (1962).
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COILLET, D., HAMANN, S. Influence of Hydrostatic Pressure on Orientation in Electrophilic Aromatic Substitutions. Nature 200, 166–167 (1963). https://doi.org/10.1038/200166b0
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DOI: https://doi.org/10.1038/200166b0
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