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New synthesis of perillene and some other furanoterpenes by cyclopropylcarbinyl rearrangement

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

Conclusions

A simple synthesis of some furanomonoterpenes, including natural perillene, was realized on the basis of the cyclopropylcarbinyl homoallylic rearrangement.

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow

    B. A. Czeskis, P. Baeckström, A. M. Moiseenkov & T. Norin

  2. Department of Organic Chemistry, Royal Institute of Technology, Stockholm, Sweden

    B. A. Czeskis, P. Baeckström, A. M. Moiseenkov & T. Norin

Authors
  1. B. A. Czeskis
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  2. P. Baeckström
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  3. A. M. Moiseenkov
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  4. T. Norin
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 144–147, January, 1989.

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Czeskis, B.A., Baeckström, P., Moiseenkov, A.M. et al. New synthesis of perillene and some other furanoterpenes by cyclopropylcarbinyl rearrangement. Russ Chem Bull 38, 131–134 (1989). https://doi.org/10.1007/BF00953717

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  • DOI: https://doi.org/10.1007/BF00953717

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