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Steric structure of 6 R-8 R'-2,9-diox A-1-azabicyclo [4.3.0]nonane derivatives

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

Conclusions

Based on the stereochemistry established for the cycloadducts obtained by the reaction of 3R-4,5-dihydro-6H-1,2-oxazine N-oxides with monosubstituted olefins it was shown that the exo approach of the olefin to the dipoles is realized exclusively in the case of styrene, and preferentially in the case of methyl acrylate and acrylonitrile.

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Literature cited

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Authors and Affiliations

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

    V. M. Shitkin, I. E. Chlenov & V. A. Tartakovskii

Authors
  1. V. M. Shitkin
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  2. I. E. Chlenov
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  3. V. A. Tartakovskii
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 211–214, January, 1977.

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Shitkin, V.M., Chlenov, I.E. & Tartakovskii, V.A. Steric structure of 6 R-8 R'-2,9-diox A-1-azabicyclo [4.3.0]nonane derivatives. Russ Chem Bull 26, 187–189 (1977). https://doi.org/10.1007/BF00921528

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  • DOI: https://doi.org/10.1007/BF00921528

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