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Mendeleev Communications, 2025, Volume 35, Issue 5, Pages 609–610
DOI: https://doi.org/10.71267/mencom.7727
(Mi mendc7279)
 

Communications

Unveiling an underestimated potential of vanillin-derived alkynes: synthesis of highly functionalized 3(2H)-furanone with antiradical activity

O. V. Shabalinaa, D. A. Shabalinb

a Irkutsk State University, 664003 Irkutsk, Russian Federation
b A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 664033 Irkutsk, Russian Federation
References:
Abstract: Target-oriented synthesis of highly functionalized 3(2H)-furanone from vanillin through several alkyne intermediates was realized in six steps. The title compound bearing two 4-hydroxy-3-methoxyphenyl moieties showed antiradical activity 1.54 times higher compared to Trolox.
Keywords: vanillin, alkynes, acetylenic ketones, 3(2H)-furanones, radical scavenging activity.
Received: 16.01.2025
Accepted: 13.03.2025
Published: 17.07.2025
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.1 Mb)


Citation: O. V. Shabalina, D. A. Shabalin, “Unveiling an underestimated potential of vanillin-derived alkynes: synthesis of highly functionalized 3(2H)-furanone with antiradical activity”, Mendeleev Commun., 35:5 (2025), 609–610
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