The reaction between perfluorobenzophenone and arom. amines proceeds with the substitution of one or more fluorine atoms. The regiochem. of this substitution is controlled by solvent polarity, temp., and nucleophilic character of the amine. O-Anilinononafluorobenzophenone can be selectively transformed into acridines or acridones by using acid or base catalysis through electrocyclization or arom. nucleophilic substitution.

Del Buttero, P., Gironda, R., Moret, M., Papagni, A., Parravicini, M., Rizzato, S., et al. (2011). Orthogonal Synthesis of Fluorinated Acridones and Acridines from Perfluorobenzophenone. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011(12), 2265-2271 [10.1002/ejoc.201001647].

Orthogonal Synthesis of Fluorinated Acridones and Acridines from Perfluorobenzophenone

GIRONDA, RAMONA;MORET, MASSIMO;PAPAGNI, ANTONIO;PARRAVICINI, MATTEO;MIOZZO, LUCIANO
2011

Abstract

The reaction between perfluorobenzophenone and arom. amines proceeds with the substitution of one or more fluorine atoms. The regiochem. of this substitution is controlled by solvent polarity, temp., and nucleophilic character of the amine. O-Anilinononafluorobenzophenone can be selectively transformed into acridines or acridones by using acid or base catalysis through electrocyclization or arom. nucleophilic substitution.
Articolo in rivista - Articolo scientifico
Nucleophilic substitution;­Pericyclic reactions;Fluorine;Nitrogen heterocycles;Solvent effects
English
2011
2011
12
2265
2271
none
Del Buttero, P., Gironda, R., Moret, M., Papagni, A., Parravicini, M., Rizzato, S., et al. (2011). Orthogonal Synthesis of Fluorinated Acridones and Acridines from Perfluorobenzophenone. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011(12), 2265-2271 [10.1002/ejoc.201001647].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/23509
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