Synthesis, Spectral Properties, and Noncovalent Bioconjugation of 1,3,5-Trinitro-2-(prop-2-yn-1-yloxy)benzene with Purine Nucleobases

Abstract A preparative method has been developed for the synthesis of 1,3,5-trinitro-2-(prop-2-yn-1-yloxy)benzene in 79% yield under mild conditions from commercially available initial compounds. The structure of the title compound has been confirmed by 1 H NMR spectroscopy. 1,3,5-Trinitro-2-(prop-2-yn-1-yloxy)benzene has been found to form noncovalent bioconjugates with DNA molecules and deoxynucleoside triphosphates. The resulting bioconjugates can be involved in click reactions with azide dyes.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s107042802560514x
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis, Spectral Properties, and Noncovalent Bioconjugation of 1,3,5-Trinitro-2-(prop-2-yn-1-yloxy)benzene with Purine Nucleobases

M. V. Bytov, O. S. Zaitseva, D. A. Kazantsev
Russian Journal of Organic Chemistry
Click Chemistry and Applications
article

Synthesis, Spectral Properties, and Noncovalent Bioconjugation of 1,3,5-Trinitro-2-(prop-2-yn-1-yloxy)benzene with Purine Nucleobases

M. V. Bytov, O. S. Zaitseva, D. A. Kazantsev
article en

Abstract

Abstract A preparative method has been developed for the synthesis of 1,3,5-trinitro-2-(prop-2-yn-1-yloxy)benzene in 79% yield under mild conditions from commercially available initial compounds. The structure of the title compound has been confirmed by 1 H NMR spectroscopy. 1,3,5-Trinitro-2-(prop-2-yn-1-yloxy)benzene has been found to form noncovalent bioconjugates with DNA molecules and deoxynucleoside triphosphates. The resulting bioconjugates can be involved in click reactions with azide dyes.

Russian Journal of Organic ChemistryVol. 61(12)
Ural State Agrarian University (RU)
Russian Science Foundation
Openalex Percentile: Top 31%
Click Chemistry and Applications
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