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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2025, том 35, выпуск 5, страницы 493–502 (Mi mendc7282)

Focus Article

The strategy of combined application of nucleophilic aromatic substitution of hydrogen (SNH ) and transition metal-catalyzed cross-coupling reactions

E. V. Verbitskiyab, V. N. Charushinab

a I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 620137 Ekaterinburg, Russian Federation
b Ural Federal University, 620002 Ekaterinburg, Russian Federation


Аннотация: Two powerful tools of organic synthesis, transition metal-catalyzed cross-coupling reactions and metal-free SNH reactions leading to nucleophilic displacement of hydrogen of the C(sp2)–H bond, have been combined into one convenient synthetic strategy. This idea has made it possible to obtain a wide variety of substituted azine derivatives, including push–pull systems, new biologically active compounds, organic semiconductors and sensor materials.

Ключевые слова: C–H functionalization, SNH reactions, Suzuki–Miyaura reaction, Buchwald–Hartwig reaction, Sonogashira reaction, Heck reaction, cross-coupling, pyrimidines, pyrazines, triazines, fused aza-aromatic compounds.

Поступила в редакцию: 26.02.2025
Принята в печать: 21.03.2025

Язык публикации: английский

DOI: 10.71267/mencom.7752



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