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Synthesis of the Promising Chiral Synthon Isopropyl-4R-Methyl-6-Iodohexanoate from L-(-)-Menthol

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Abstract

A synthesis of the promising optically pure synthon isopropyl-4R-methyl-6-iodohexanoate based on ozonolytic transformation of the product of regiospecific dehydratation of L-(-)-menthol, (R)-p-menth-3-ene, into 2,6R-dimethyl-8-hydroxyoctan-3-one was proposed.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Ufa Scientific Center, Russian Academy of Sciences, RF, 450054, Ufa, prospekt Oktyabrya, 71, Russia

    G. Yu. Ishmuratov, M. P. Yakovleva, R. R. Muslukhov & G. A. Tolstikov

  2. Birsk State Pedagogic Institute, RF, 452320, Birsk, ul. Internatsional’naya, 10, Russia

    V. A. Ganieva

Authors
  1. G. Yu. Ishmuratov
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  2. M. P. Yakovleva
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  3. V. A. Ganieva
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  4. R. R. Muslukhov
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  5. G. A. Tolstikov
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Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 33–36, January–February, 2005.

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Ishmuratov, G.Y., Yakovleva, M.P., Ganieva, V.A. et al. Synthesis of the Promising Chiral Synthon Isopropyl-4R-Methyl-6-Iodohexanoate from L-(-)-Menthol. Chem Nat Compd 41, 41–44 (2005). https://doi.org/10.1007/s10600-005-0070-6

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  • DOI: https://doi.org/10.1007/s10600-005-0070-6

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