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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2007, том 17, выпуск 1, страницы 52–53 (Mi mendc3375)

Эта публикация цитируется в 16 статьях

Stereoselective synthesis of N-unsubstituted pyrazolidines from 3-nitro-2-trichloromethyl-2H-chromenes and hydrazine hydrate

V. Yu. Korotaeva, I. B. Kutyasheva, V. Ya. Sosnovskikha, M. I. Kodessb

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

Аннотация: The reaction of 3-nitro-2-trichloromethyl-2H-chromenes with hydrazine hydrate in ethanol at room temperature results in 3,4-trans, 4,5-trans-3-(2-hydroxyaryl)-4-nitro-5-trichloromethylpyrazolidines in 56–73% yields; the structures of these compounds were established by 1H NMR, 2D COSY and 2D NOESY spectra.

Язык публикации: английский

DOI: 10.1016/j.mencom.2007.01.021



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