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Synthesis of model dimers of lignin from (1-hydroxyalkyl)phenols

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Chemistry of Natural Compounds Aims and scope

Abstract

It has been shown that model (1-hydroxyalkyl)phenols of lignin condense in an acid medium with heating to form dimers of the indan and Ar-C3-Ar series, depending on the substituents in the aromatic ring.

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Literature cited

  1. L. S. Smirnova, S. Mukhamedova, and Kh. A. Abduazimov, Khim. Prir. Soedin., 732 (1991).

  2. G. F. Zakis, Synthesis of Model Compounds of Lignin [in Russian], Riga (1980), pp. 102, 195.

  3. G. V. Dobele, T. N. Skripchenko, G. É. Domburg, M. G. Liepin'sh, and T. N. Osadshaya, Khim. Drev., No. 6, 83 (1988).

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Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 564–567, September–October, 1992.

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Smirnova, L.S., Abduazimov, K.A. Synthesis of model dimers of lignin from (1-hydroxyalkyl)phenols. Chem Nat Compd 28, 493–495 (1992). https://doi.org/10.1007/BF00630660

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  • DOI: https://doi.org/10.1007/BF00630660

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