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Synthesis of phosphonates immobilized on a polycyclic platform and conjugated with triazole moieties

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Abstract

Oligofunctionalized 1,1′-methylenedinaphthalenes and rctt-o-methyltetra(C-naphthyl)-resorcincalix[4]arenes, wherein exocyclic substituents contain phosphonate and terminal triazole moieties linked via spacers of the different steric hindrance, were synthesized, isolated in high yields, and characterized. In all the cases, the key step was the so-called “click” reaction of catalytic azide—alkyne cycloaddition.

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Authors and Affiliations

  1. Institute of Biology and Chemistry, Moscow Pedagogical State University, 6 ul. Kibalchicha, 129164, Moscow, Russian Federation

    O. S. Serkova, V. V. Glushko & V. I. Maslennikova

  2. Institute of Biomedical Chemistry, Build. 8, 10 ul. Pogodinskaya, 119121, Moscow, Russian Federation

    I. Yu. Toropygin

Authors
  1. O. S. Serkova
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  2. V. V. Glushko
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  3. I. Yu. Toropygin
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  4. V. I. Maslennikova
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Corresponding author

Correspondence to V. I. Maslennikova.

Additional information

Based on the materials of the II Scientific Conference “Dynamic Processes in the Chemistry of Organoelement Compounds” (November 11–13, 2020, Kazan, Russia).

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1328–1334, July, 2021.

This work was carried out within the framework of the State Assignment of the Ministry of Science and Higher Education of the Russian Federation (Project No. AAAA-A21-121011190029-1).

This paper does not contain descriptions of studies on animals or humans.

The authors declare no competing interests.

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Serkova, O.S., Glushko, V.V., Toropygin, I.Y. et al. Synthesis of phosphonates immobilized on a polycyclic platform and conjugated with triazole moieties. Russ Chem Bull 70, 1328–1334 (2021). https://doi.org/10.1007/s11172-021-3219-y

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  • DOI: https://doi.org/10.1007/s11172-021-3219-y

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