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Radical-cations of 3,6-di-tert-butylpyrocatechol esters

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    Conformational transitions characteristic of nonplanar rings were detected in the radical-cation of the 3,6-di-tert-butylpyrocatechol ester of ethylene glycol.

  2. 2.

    Cyclic radical-cations are formed during the oxidation of 2-acyloxyphenols.

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Literature cited

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow

    N. A. Malysheva, A. I. Prokof'ev, N. N. Bubnov, S. P. Solodovnikov, T. I. Prokof'eva, V. B. Vol'eva, V. V. Ershov & M. I. Kabachnik

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  1. N. A. Malysheva
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  2. A. I. Prokof'ev
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  3. N. N. Bubnov
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  4. S. P. Solodovnikov
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  5. T. I. Prokof'eva
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  6. V. B. Vol'eva
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  7. V. V. Ershov
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  8. M. I. Kabachnik
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1040–1047, May, 1988.

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Malysheva, N.A., Prokof'ev, A.I., Bubnov, N.N. et al. Radical-cations of 3,6-di-tert-butylpyrocatechol esters. Russ Chem Bull 37, 907–914 (1988). https://doi.org/10.1007/BF00957058

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  • DOI: https://doi.org/10.1007/BF00957058

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