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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 6, страницы 687–696 (Mi mendc1294)

Эта публикация цитируется в 4 статьях

Focus Article

Acetylenes and nitriles as unconventional reactants for aza-Wittig reactions

H. B. Tukhtaeva, I. D. Sorokina, M. Ya. Melnikova, E. M. Budyninaab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b P.N. Lebedev Physical Institute, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: The classic version of aza-Wittig reactions, namely, reactions between phosphazenes and compounds with polar double bonds, is widely employed in organic synthesis to produce C=N bonds. However, only a limited number of aza-Wittig reactions between phosphazenes and compounds with triple bonds is known, which has a lot to do with certain structural features of the reactants, wherein additional activation is required. This review provides a guide to those rare examples of aza-Wittig reactions with acetylenes and nitriles. A unique trait of these atom-economic processes is that they afford Wittig or new aza-Wittig reagents, respectively, which offers new opportunities for employing these reactions in organic syntheses, especially those of N-heterocyclic compounds.

Ключевые слова: aza-Wittig reaction, phosphazenes, acetylenes, nitriles, N-heterocyclic compounds.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.11.001



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