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Reactivities of 1-mono- and 1,1′-bis-p-nitrophenylferrocenes and of 1,1′-diacetylferrocene

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    The introduction of acetyl and p-nitrophenyl groups into the ferrocene nucleus greatly reduces the ability of hydrogens of the ferrocene nucleus to undergo aromatic-substitution reactions (arylation with diazo compounds, mercuration, and acylation).

  2. 2.

    Reaction of diacetylferrocene with diazo compounds leads to breakdown of the ferrocene nucleus and formation of substances considered tentatively to be acetyl(arylazo)cyclopentadienes.

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Nesmeyanov, A.N., Perevalova, E.G., Golovnya, R.V. et al. Reactivities of 1-mono- and 1,1′-bis-p-nitrophenylferrocenes and of 1,1′-diacetylferrocene. Russ Chem Bull 6, 647–649 (1957). https://doi.org/10.1007/BF01169284

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  • DOI: https://doi.org/10.1007/BF01169284

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