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Oxidative transformations of 4-(Ω-hydroxyalkyl)-2,6-di-tert-butylphenols

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Conclusions

Methylenequinones obtained by the oxidation of 4-Ω-hydroxyalkyl-2,6-di-tert-butyl-phenols undergo inter- and intramolecular transformations to give oligomers or tetra-hydrofuran and hydroxyketone derivatives depending on the position of the hydroxyl group in the aliphatic chain of the para substituent.

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Literature cited

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Russia

    A. P. Krysin & A. N. Fedorenko

Authors
  1. A. P. Krysin
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  2. A. N. Fedorenko
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1671–1674, July, 1989.

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Krysin, A.P., Fedorenko, A.N. Oxidative transformations of 4-(Ω-hydroxyalkyl)-2,6-di-tert-butylphenols. Russ Chem Bull 38, 1533–1536 (1989). https://doi.org/10.1007/BF00978453

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  • DOI: https://doi.org/10.1007/BF00978453

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