Nucleophilic Substitution of Chloro-Substituted Enaminones that are Derivatives of Imidazolidine Nitroxides − The Catalytic Effect of the Cyanide Ion

Nucleophilic Substitution of Chloro-Substituted Enaminones that are Derivatives of Imidazolidine Nitroxides − The Catalytic Effect of the Cyanide Ion

The cyanide ion is a catalyst for reactions of nucleophiles with chloro‐substituted enaminones derived from imidazolidine nitroxides, which result in the formation of formal nucleophilic substitution products. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

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Veröffentlicht in:European journal of organic chemistry 2003-09, Vol.2003 (18), p.3599-3602
Hauptverfasser: Roshchupkina, Galina I., Rybalova, Tatyana V., Gatilov, Yury V., Reznikov, Vladimir A.
Format: Artikel
Sprache:eng
Schlagworte:
Enaminones
Nitrogen heterocycles
Nitroxides
Nucleophilic substitution
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Zusammenfassung:The cyanide ion is a catalyst for reactions of nucleophiles with chloro‐substituted enaminones derived from imidazolidine nitroxides, which result in the formation of formal nucleophilic substitution products. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.200200722