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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2025, том 35, выпуск 5, страницы 609–610 (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


Аннотация: 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.

Ключевые слова: vanillin, alkynes, acetylenic ketones, 3(2H)-furanones, radical scavenging activity.

Поступила в редакцию: 16.01.2025
Принята в печать: 13.03.2025

Язык публикации: английский

DOI: 10.71267/mencom.7727



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