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Cyclocondensation of 3-aryl-2-cyano-2-butenoic acid esters with schiff bases

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The condensation of ethyl 3-aryl-2-cyano-2-butenoates with benzylideneanilines in the presence of aluminum chloride affords 1,4,6-triaryl-2-oxo-1,2,5,6-tetrahydropyridine-2-carbonitriles; the reaction with hydrobenzamide gives N-unsubstituted tetrahydropyridine.

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Authors and Affiliations

  1. Kl. Okhridski Sofia University, 1126, Sofia, People's Republic of Bulgaria

    Ts. P. Cholakova & Kh. Ivanov

Authors
  1. Ts. P. Cholakova
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  2. Kh. Ivanov
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 209–211, February, 1988.

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Cholakova, T.P., Ivanov, K. Cyclocondensation of 3-aryl-2-cyano-2-butenoic acid esters with schiff bases. Chem Heterocycl Compd 24, 173–175 (1988). https://doi.org/10.1007/BF00473327

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  • DOI: https://doi.org/10.1007/BF00473327

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