Chemistry of Natural Compounds

, Volume 53, Issue 2, pp 231–233 | Cite as

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

  • G. Yu. Ishmuratov
  • M. P. Yakovleva
  • V. A. Vydrina
  • M. A. Rubleva
  • N. M. Ishmuratova
  • A. G. Tolstikov
Article
  • 42 Downloads

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.

Keywords

methyl ricinoleate castor oil O,N-containing macroheterocycles esters hydrazone and azine moieties synthesis 

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Copyright information

© Springer Science+Business Media New York 2017

Authors and Affiliations

  • G. Yu. Ishmuratov
    • 1
  • M. P. Yakovleva
    • 1
  • V. A. Vydrina
    • 1
  • M. A. Rubleva
    • 1
  • N. M. Ishmuratova
    • 1
  • A. G. Tolstikov
    • 1
  1. 1.Ufa Institute of ChemistryUfaRussian Federation

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