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[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles

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Chemistry of Natural Compounds Aims and scope

The reactivities of the keto analogs of methyl ricinolate and its triglyceride with hydrazine hydrate were studied. The ester was found to be inert, which made it possible to synthesize a macrocyclic azine with a side chain hydrazone moiety from a 12-oxo-derivative.

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References

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Authors and Affiliations

  1. Ufa Institute of Chemistry, 71 Prosp. Oktyabrya, Ufa, Russian Federation, 450054

    G. Yu. Ishmuratov, M. P. Yakovleva, V. A. Vydrina, M. A. Rubleva, N. M. Ishmuratova & A. G. Tolstikov

Authors
  1. G. Yu. Ishmuratov
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  2. M. P. Yakovleva
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  3. V. A. Vydrina
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  4. M. A. Rubleva
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  5. N. M. Ishmuratova
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  6. A. G. Tolstikov
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Corresponding author

Correspondence to M. P. Yakovleva.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 2, March–April, 2017, pp. 199–201.

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Ishmuratov, G.Y., Yakovleva, M.P., Vydrina, V.A. et al. [1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles. Chem Nat Compd 53, 231–233 (2017). https://doi.org/10.1007/s10600-017-1959-6

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  • DOI: https://doi.org/10.1007/s10600-017-1959-6

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