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Reaction of 2,9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with boron fluoride etherate

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

Conclusions

  1. 1.

    The direction of the reaction of boron fluoride etherate with 6,8-disubstituted 2,9-dioxa-1-azabicyelo-[4.3.0]nonanes depends on the nature and spatial arrangement of the substitatnts.

  2. 2.

    The first member of a new heterocyclic system was obtained, namely a spiro(isoxazolidine-3,2′-tetrahydrofuran) derivative.

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Literature cited

  1. I. E. Chlenov, L. N. Kolymagina, and V. A. Tartakovskii, Izv. Akad. Nauk SSSR, Ser. Khim.,1972, 893.

  2. F. Caruso, G. Cum, and N. Ucella, Tetrahedron Lett.,1971, 3711.

  3. I. E. Chlenov, I. M. Petrova, and V. A. Tartakovskii, Izv. Akad. Nauk SSSR, Ser. Khim.,1974, 2651.

  4. I. E. Chlenov, V. I. Khudak, L. N. Kolymagina, N. S. Morozova, and V. A. Tartakovskii, Izv. Akad. Nauk SSSR, Ser. Khim.,1970, 4867.

  5. I. E. Chlenov, I. M. Petrova, V. M. Shitkin, and V. A. Tartakovskii, Izv. Akad. Nauk SSSR, Ser. Khim.,1976, 1405.

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Authors and Affiliations

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

    I. E. Chlenov, Yu. B. Salamonov, B. N. Khasapov, N. F. Karpenko, O. S. Chizhov & V. A. Tartakovskii

Authors
  1. I. E. Chlenov
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  2. Yu. B. Salamonov
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  3. B. N. Khasapov
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  4. N. F. Karpenko
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  5. O. S. Chizhov
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  6. V. A. Tartakovskii
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2830–2833, December, 1977.

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Chlenov, I.E., Salamonov, Y.B., Khasapov, B.N. et al. Reaction of 2,9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with boron fluoride etherate. Russ Chem Bull 26, 2619–2622 (1977). https://doi.org/10.1007/BF00924588

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  • DOI: https://doi.org/10.1007/BF00924588

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