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Highly selective method for the synthesis of substituted alkylpyridines

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

Conclusions

A highly selective method was developed for the synthesis of substituted alkylpyridines by the reactions of ethynylcarbinols and vinylacetylenes with carboxylic acid chlorides and ammonia in the presence of zinc chloride. The intermediate formation of pyrylium salts was demonstrated.

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Authors and Affiliations

  1. Institute of Chemistry, Bashkir Scientific Center, Urals Branch, Academy of Sciences of the USSR, Ufa

    U. M. Dzhemilev, F. A. Selimov & O. G. Rutman

Authors
  1. U. M. Dzhemilev
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  2. F. A. Selimov
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  3. O. G. Rutman
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2600–2604, November, 1988.

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Dzhemilev, U.M., Selimov, F.A. & Rutman, O.G. Highly selective method for the synthesis of substituted alkylpyridines. Russ Chem Bull 37, 2343–2346 (1988). https://doi.org/10.1007/BF00959892

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  • DOI: https://doi.org/10.1007/BF00959892

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