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Organocatalytic Enamine–Azide Addition Reaction in the Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles

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Abstract

A high efficiency of diethanolamine as organocatalyst in the cycloaddition of organic (including heterocyclic) mono-, di-, and triazides to active methylene compounds has been demonstrated. As a result, a number of functionally substituted bi- and polycyclic systems have been synthesized.

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Funding

This study was performed under financial support by the Russian Foundation for Basic Research and by the Govern­ment of Irkutsk oblast (project no. 20-43-383003 r_mol_a).

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Authors and Affiliations

  1. Irkutsk State University, 664003, Irkutsk, Russia

    T. V. Sokolnikova, A. G. Proidakov & V. N. Kizhnyaev

Authors
  1. T. V. Sokolnikova
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  2. A. G. Proidakov
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  3. V. N. Kizhnyaev
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Corresponding author

Correspondence to T. V. Sokolnikova.

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The authors declare the absence of conflict of interest.

Additional information

Translated from Zhurnal Organicheskoi Khimii, 2021, Vol. 57, No. 3, pp. 400–409 https://doi.org/10.31857/S0514749221030083.

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Sokolnikova, T.V., Proidakov, A.G. & Kizhnyaev, V.N. Organocatalytic Enamine–Azide Addition Reaction in the Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles. Russ J Org Chem 57, 376–382 (2021). https://doi.org/10.1134/S1070428021030088

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