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Specific Features of the Reactions of Pentaphenylantimony with Polyfunctional Heterocyclic Carboxylic Acids

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Abstract

Pyridine-2,6- and 2,5-dicarboxylic acids have acted as bifunctional compounds in the reactions with pentaphenylantimony, forming bis(tetraphenylantimony)pyridine-2,6- and 2,5-dicarboxylate, respectively. The interaction of pentaphenylantimony with 2-[(6-hydroxy-5-nitroso-4(3H)-oxopyrimidin-2-yl)sulfanyl]acetic acid involving carboxyl and hydroxyl groups in the pyrimidine ring has afforded 2-{[5-nitroso-4(3H)-oxo-6-(tetraphenylstiboxy)pyrimidin-2-yl]sulfanyl}tetraphenylantimony acetate. The structural features of the synthesized compounds have been established by means of X-ray diffraction analysis.

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Funding

This study was financially supported by the Russian Foundation for Basic Research (project no. 19-33-90061).

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  1. National Research South Ural State University, 454080, Chelyabinsk, Russia

    Yu. O. Gubanova, V. V. Sharutin, O. K. Sharutina & K. Yu. Petrova

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  1. Yu. O. Gubanova
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  2. V. V. Sharutin
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  3. O. K. Sharutina
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Correspondence to Yu. O. Gubanova.

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Gubanova, Y.O., Sharutin, V.V., Sharutina, O.K. et al. Specific Features of the Reactions of Pentaphenylantimony with Polyfunctional Heterocyclic Carboxylic Acids. Russ J Gen Chem 90, 1664–1669 (2020). https://doi.org/10.1134/S1070363220090121

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  • DOI: https://doi.org/10.1134/S1070363220090121

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