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First synthesis of p-mentha-1,8-diene triol

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Abstract

The first synthesis of p-mentha-1,8-diene triol from (−)-verbenone included obtaining pinane epoxy diol and its subsequent acid-catalyzed rearrangement on montmorillonite clay as the key steps.

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Authors and Affiliations

  1. N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent’eva, 630090, Novosibirsk, Russian Federation

    O. V. Ardashov, O. S. Mikhal’chenko, D. V. Korchagina, K. P. Volcho & N. F. Salakhutdinov

  2. Novosibirsk State University, 2 ul. Pirogova, 630090, Novosibirsk, Russian Federation

    E. V. Khaid

Authors
  1. O. V. Ardashov
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  2. E. V. Khaid
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  3. O. S. Mikhal’chenko
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  4. D. V. Korchagina
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  5. K. P. Volcho
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  6. N. F. Salakhutdinov
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Corresponding author

Correspondence to K. P. Volcho.

Additional information

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 0172–0175, January, 2013.

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Ardashov, O.V., Khaid, E.V., Mikhal’chenko, O.S. et al. First synthesis of p-mentha-1,8-diene triol. Russ Chem Bull 62, 171–174 (2013). https://doi.org/10.1007/s11172-013-0025-1

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  • DOI: https://doi.org/10.1007/s11172-013-0025-1

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