[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles
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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.
Keywordsmethyl ricinoleate castor oil O,N-containing macroheterocycles esters hydrazone and azine moieties synthesis
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