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[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles
- Ishmuratov, G. Yu., Yakovleva, M. P., Vydrina, V. A., Rubleva, M. A., Ishmuratova, N. M., Tolstikov, A. G.
- Chemistry of natural compounds 2017 v.53 no.2 pp. 231-233
- chemistry, hydrazine, ricinoleic acid, triacylglycerols
- 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.