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Investigation of cyclic acetals of substituted benzaldehydes forming a dioxane ring by1H and13C NMR spectroscopy

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

Conclusions

  1. 1.

    The methods of1H and13C NMR have been employed to study the effect of various substituants in the aromatic ring on the chemical shifts of the protons and carbon nuclei of the dioxane and aromatic rings in a number of 2-aryl-4-methyl-1,3-dioxanes.

  2. 2.

    A substituent on the aromatic ring has the strongest effect on 2-H and 2-C.

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Authors and Affiliations

  1. Institute of Chemical Physics of the Academy of Sciences of the USSR, Moscow

    V. P. Lezina, A. U. Stepanyants, F. A. Alimirzoev, S. S. Zlotskii & D. L. Rakhmankulov

  2. Ufa Petroleum Institute, USSR

    V. P. Lezina, A. U. Stepanyants, F. A. Alimirzoev, S. S. Zlotskii & D. L. Rakhmankulov

Authors
  1. V. P. Lezina
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  2. A. U. Stepanyants
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  3. F. A. Alimirzoev
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  4. S. S. Zlotskii
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  5. D. L. Rakhmankulov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 792–798, April, 1976.

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Lezina, V.P., Stepanyants, A.U., Alimirzoev, F.A. et al. Investigation of cyclic acetals of substituted benzaldehydes forming a dioxane ring by1H and13C NMR spectroscopy. Russ Chem Bull 25, 772–777 (1976). https://doi.org/10.1007/BF00922377

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  • DOI: https://doi.org/10.1007/BF00922377

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