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// 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. Musikhina
ab
,
I. A. Utepova
ab
,
O. N. Chupakhin
ab
,
A. I. Suvorova
b
,
E. Yu. Zyryanova
b
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 (Ac
2
O/AlCl
3
) reaction of azinylferrocenes occurs regioselectively at position 1′. Acetylated derivatives upon reaction with Ph
3
P=CH
2
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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Supplementary materials:
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, 2026