The CuOAc-mediated N-arylation of 1H-indole derivatives and 1H-carbazole with aryl iodides under base-free and ligandless conditions provides with complete N-selectivity the required N-arylazoles in moderate to good yields. The experimental conditions of this new version of the Ullmann reaction allow an unprecedent tolerance of functional groups and facilitate the work-up of the reaction mixtures and isolation of the required chemically pure reaction products.

Selective, efficient and functional group-tolerant CuOAc-mediated N-arylation of 1H-indoles and 9H-carbazole with aryl iodides under base-free and ligandless conditions

BELLINA, FABIO;ROSSI, RENZO
2007-01-01

Abstract

The CuOAc-mediated N-arylation of 1H-indole derivatives and 1H-carbazole with aryl iodides under base-free and ligandless conditions provides with complete N-selectivity the required N-arylazoles in moderate to good yields. The experimental conditions of this new version of the Ullmann reaction allow an unprecedent tolerance of functional groups and facilitate the work-up of the reaction mixtures and isolation of the required chemically pure reaction products.
2007
Bellina, Fabio; C., Calandri; S., Cauteruccio; Rossi, Renzo
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/179554
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