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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2020 Volume 30, Issue 2, Pages 209–210 (Mi mendc1150)

This article is cited in 4 papers

Communications

Regioselective synthesis of 1-azinyl-1′-isopropenylferrocenes

A. A. Musikhinaab, I. A. Utepovaab, O. N. Chupakhinab, A. I. Suvorovab, E. Yu. Zyryanovab

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

Abstract: The Friedel–Crafts acetylation (Ac2O/AlCl3) reaction of azinylferrocenes occurs regioselectively at position 1′. Acetylated derivatives upon reaction with Ph3P=CH2 give the corresponding 1-azinyl-1′-isopropenylferrocenes.

Keywords: ferrocenes, isopropenylferrocene, regioselective synthesis, Friedel–Crafts acylation, Wittig reaction, azines.

Language: English

DOI: 10.1016/j.mencom.2020.03.026



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