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Regioselective synthesis of 1-azinyl-1′-isopropenylferrocenes
[Display omitted] 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.
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Published in: | Mendeleev communications 2020-03, Vol.30 (2), p.209-210 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
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. |
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ISSN: | 0959-9436 |
DOI: | 10.1016/j.mencom.2020.03.026 |