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Diene condensation of allylacetylene and allylethynyldimethylcarbinol with cyclopentadiene and some transformations of the obtained adducts

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

Conclusions

The diene condensation of allylacetylene and allylethynyldimethylcarbinol with cyclopentadiene proceeds, as in the case of hexachlorocyclopentadiene, with involvement of the vinyl group, but under more drastic conditions and with the formation of both the mono- and the bisadducts.

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Literature cited

  1. M. G. Veliev, M. M. Guseinov, L. A. Yanovskaya, é. Sh. Mamedov, and A. A. Bairamov, Izv. Akad. Nauk SSSR, Ser. Khim.,1980, 932.

  2. M. S. Malinovskii, M. P. Khmel, N. N. Baranov, and N. G. Krivosheeva, Ukr. Khim. Zh.,16, 1064 (1975).

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Authors and Affiliations

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

    M. G. Veliev, M. M. Guseinov, L. A. Yanovskaya & R. F. Gakhramanov

  2. Institute of Chloroorganic Synthesis, Academy of Sciences of the Azerbaidzhan SSR, Sumgait

    M. G. Veliev, M. M. Guseinov, L. A. Yanovskaya & R. F. Gakhramanov

Authors
  1. M. G. Veliev
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  2. M. M. Guseinov
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  3. L. A. Yanovskaya
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  4. R. F. Gakhramanov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 144–149, January, 1981.

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Veliev, M.G., Guseinov, M.M., Yanovskaya, L.A. et al. Diene condensation of allylacetylene and allylethynyldimethylcarbinol with cyclopentadiene and some transformations of the obtained adducts. Russ Chem Bull 30, 121–127 (1981). https://doi.org/10.1007/BF00962267

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  • DOI: https://doi.org/10.1007/BF00962267

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