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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2017 Volume 27, Issue 3, Pages 228–230 (Mi mendc1950)

This article is cited in 19 papers

Communications

Synthesis and antimitotic activity of novel 5-aminoisoxazoles bearing alkoxyaryl moieties

D. A. Vasilenkoa, E. B. Averinaab, N. A. Zefirova, B. Wobithc, Yu. K. Grishina, V. B. Rybakova, O. N. Zefirovaab, T. S. Kuznetsovaa, S. A. Kuznetsovc, N. S. Zefirovab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
c Institute of Biological Sciences, Cell Biology and Biosystems Technology, University of Rostock, Rostock, Germany

Abstract: 5-Aminoisoxazoles containing trimethoxy- and methylenedioxyphenyl moieties were prepared by heterocyclization of electrophilic alkenes with tetranitromethane in the presence of triethylamine with subsequent reduction of resulting 5-nitroisoxazoles. The crystal structure of 3,4,5-trimethoxybenzyl 5-aminoisoxazole-3-carboxylate was determined by X-ray analysis. Two novel 5-aminoisoxazoles demonstrated moderate antimitotic activity to human lung carcinoma A549 cell line.

Language: English

DOI: 10.1016/j.mencom.2017.05.003



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