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Synthesis of monocationic β-cyclodextrin derivatives

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Abstract

Reactions of 6-bromo- and 6-iodo-6-deoxy-β-cyclodextrin with organic amines of diverse nature afforded a series of monocationic derivatives with aminium groups located in the cyclodextrin scaffold on the side of the primary hydroxy groups. The structure and composition of the obtained cationic β-cyclodextrin derivatives were confirmed by 1H and 13C NMR data.

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Authors and Affiliations

  1. Institute of Biology and Chemistry, Moscow State University of Education, Nesvizhskii per. 3, Moscow, 119021, Russia

    D. A. Shipilov, G. I. Kurochkina, M. A. Malenkovskaya & M. K. Grachev

  2. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, Russia

    I. I. Levina

Authors
  1. D. A. Shipilov
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  2. G. I. Kurochkina
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  3. I. I. Levina
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  4. M. A. Malenkovskaya
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  5. M. K. Grachev
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Corresponding author

Correspondence to D. A. Shipilov.

Additional information

Original Russian Text © D.A. Shipilov, G.I. Kurochkina, I.I. Levina, M.A. Malenkovskaya, M.K. Grachev, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 2, pp. 290–294.

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Shipilov, D.A., Kurochkina, G.I., Levina, I.I. et al. Synthesis of monocationic β-cyclodextrin derivatives. Russ J Org Chem 53, 290–295 (2017). https://doi.org/10.1134/S1070428017020257

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  • DOI: https://doi.org/10.1134/S1070428017020257

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