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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 4, страницы 485–486 (Mi mendc1231)

Эта публикация цитируется в 2 статьях

Communications

Pseudonitrosites as masked nitroalkenes in the Barton–Zard pyrrole synthesis

D. A. Rusanovab, A. B. Myshlyavtsevab, E. A. Silyanovaa, A. V. Sameta, V. V. Semenova

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation


Аннотация: 3-Aryl-4-methylpyrrole-2-carboxylates were prepared via the Barton–Zard reaction using pseudonitrosites as a source of the corresponding nitroalkenes. The starting pseudonitrosites were, in turn, obtained via addition of N2O3 to propenylbenzenes available from the natural plant essential oils.

Ключевые слова: Barton–Zard reaction, pseudonitrosites, propenylbenzenes, isomerization, pyrroles, lamellarins.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.07.026



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