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Insect pheromones and their analogues XXV. Synthesis of acetylenic precursors of pheromones from undecylenic acid

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Abstract

The selective ozonolysis of pentadec-1-en-12-yne and heptadec-1-en-12-yne, synthesized from the readily available undecylenic acid, has given tetradec- and hexadec-11-yn-1-ols — acetylenic precursors of a number of pheromones of insects of the order Lepidoptera.

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Authors
  1. V. N. Odinokov
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  2. G. Yu. Ishmuratov
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  3. I. M. Ladenkova
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  4. E. M. Vyrypaev
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  5. G. A. Tolstikov
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Additional information

Institute of Chemistry, Bashkir Scientific Center, Urals Branch, Academy of Sciences of the USSR, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 823–825, November–December, 1990.

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Odinokov, V.N., Ishmuratov, G.Y., Ladenkova, I.M. et al. Insect pheromones and their analogues XXV. Synthesis of acetylenic precursors of pheromones from undecylenic acid. Chem Nat Compd 26, 702–704 (1990). https://doi.org/10.1007/BF00630085

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  • DOI: https://doi.org/10.1007/BF00630085

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