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Synthesis of new p-tert-butylcalix[4]arene derivatives containing photopolymerizable 1,3-butadiyne fragments

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Abstract

Successive functionalization of p-tert-butylcalix[4]arene afforded a bifunctional derivative containing photopolymerizable pentacosa-10,12-diynoic acid fragments on the upper rim and propargyl groups on the lower rim of the macrocycle having a cone structure. The functionalization can be readily accomplished via copper-catalyzed azide–alkyne cycloaddition under mild conditions.

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Authors and Affiliations

  1. Kazan (Volga region) Federal University, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008, Russia

    V. A. Burilov, A. M. Valiyakhmetova, R. I. Aukhadieva, S. E. Solovieva & I. S. Antipin

  2. Arbuzov Institute of Organic and Physical Chemistry, Kazan Research Center, Russian Academy of Sciences, ul. Arbuzova 8, Kazan, Tatarstan, 420008, Russia

    S. E. Solovieva & I. S. Antipin

Authors
  1. V. A. Burilov
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  2. A. M. Valiyakhmetova
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  3. R. I. Aukhadieva
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  4. S. E. Solovieva
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  5. I. S. Antipin
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Correspondence to V. A. Burilov.

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Dedicated to V.F. Mironov on His 60th Anniversary

Original Russian Text © V.A. Burilov, A.M. Valiyakhmetova, R.I. Aukhadieva, S.E. Solovieva, I.S. Antipin, 2017, published in Zhurnal Obshchei Khimii, 2017, Vol. 87, No. 9, pp. 1463–1468.

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Burilov, V.A., Valiyakhmetova, A.M., Aukhadieva, R.I. et al. Synthesis of new p-tert-butylcalix[4]arene derivatives containing photopolymerizable 1,3-butadiyne fragments. Russ J Gen Chem 87, 1946–1951 (2017). https://doi.org/10.1134/S1070363217090092

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  • DOI: https://doi.org/10.1134/S1070363217090092

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