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13C NMR spectra of substituted cyclopropanes

3. Gem-Dichlorocylopropyl aryl ethers

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

Conclusions

  1. 1.

    Study has been made of the13C NMR spectra of various gem-dichlorocyclopropyl aryl ethers and their bridged system analogs, pgp-σπ-pπ coupling is not established in cyclopropyl ethers containing substituents capable of undergoing coupling.

  2. 2.

    The conformations proposed for these compounds are quite consistent with the experimental data.

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Authors and Affiliations

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

    D. F. Kushnarev, A. A. Retinskii, G. A. Kalabin & S. M. Shostakovskii

  2. Institute of Oil and Coal Synthesis, A. A. Zhdanov Irkutsk State university, USSR

    D. F. Kushnarev, A. A. Retinskii, G. A. Kalabin & S. M. Shostakovskii

Authors
  1. D. F. Kushnarev
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  2. A. A. Retinskii
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  3. G. A. Kalabin
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  4. S. M. Shostakovskii
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 594–601, March, 1977.

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Kushnarev, D.F., Retinskii, A.A., Kalabin, G.A. et al. 13C NMR spectra of substituted cyclopropanes. Russ Chem Bull 26, 533–538 (1977). https://doi.org/10.1007/BF01179461

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  • DOI: https://doi.org/10.1007/BF01179461

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