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Alkylation of isobornylphenols with styrene in the presence of p-toluenesulfonic acid

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Abstract

The alkylation of racemic isobornylphenols with styrene in the presence of p-toluenesulfonic acid (5 mol %) afforded new hybrid compounds combining bulky terpene and phenylethyl fragments in a single molecule.

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Authors and Affiliations

  1. Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, Syktyvkar, 167982, Russia

    I. Yu. Chukicheva, O. V. Sukrusheva & A. V. Kutchin

Authors
  1. I. Yu. Chukicheva
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  2. O. V. Sukrusheva
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  3. A. V. Kutchin
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Correspondence to O. V. Sukrusheva.

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Original Russian Text © I.Yu. Chukicheva, O.V. Sukrusheva, A.V. Kutchin, 2015, published in Zhurnal Obshchei Khimii, 2015, Vol. 85, No. 6, pp. 929–932.

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Chukicheva, I.Y., Sukrusheva, O.V. & Kutchin, A.V. Alkylation of isobornylphenols with styrene in the presence of p-toluenesulfonic acid. Russ J Gen Chem 85, 1397–1400 (2015). https://doi.org/10.1134/S1070363215060079

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  • DOI: https://doi.org/10.1134/S1070363215060079

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