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Insect pheromones and their analogues. XLVI. Synthesis of 13RS-hydrooxytetradec-5Z-enoic acid — The acyclic precursor of the macrolide component of the pheromone of Cryptolestes pusillus

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Abstract

New routes for the synthesis of 13RS-hydroxytetradec-5Z-enoic acid — the acyclic precursor of the macrolide component of the pheromone ofCryptolestes pusillus have been developed on the basis of the readily accessible 1-methylcycloocta-1Z, 5Z-diene or isopropyl nona-3E,8-dienoate.

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Authors
  1. V. N. Odinokov
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  2. G. Yu. Ishmuratov
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  3. O. V. Sokol'skaya
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  4. L. Yu. Gubaidullin
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  5. R. R. Muslukhov
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  6. G. A. Tolstikov
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Additional information

Institute of Biological Plant Protection, Moldovian Academy of Sciences, Kishinev. Scientific-Research Institute of Forestry and Forestry Mechanization, Pushkino. Moscow Institute of Wood Technology; and Georgia Institute of Mountain Forestry, Tbilisi. Translated from Khimiya Prirodnykh Soedeninii, No. 1, pp. 150–155, January–February, 1993.

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Odinokov, V.N., Ishmuratov, G.Y., Sokol'skaya, O.V. et al. Insect pheromones and their analogues. XLVI. Synthesis of 13RS-hydrooxytetradec-5Z-enoic acid — The acyclic precursor of the macrolide component of the pheromone of Cryptolestes pusillus. Chem Nat Compd 29, 128–131 (1993). https://doi.org/10.1007/BF00631039

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  • DOI: https://doi.org/10.1007/BF00631039

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