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Unsymmetrical Aryl-Aryl Cross-Coupling Leading to 6H-Dibenzopyrans

Authors :
Marta Catellani
Elena Motti
Raffaella Ferraccioli
Nicola Della Ca
Source :
Synthesis (Stuttg.) 6 (2008): 995–997. doi:10.1055/s-2007-990934, info:cnr-pdr/source/autori:Elena Motti (1); Nicola Della Ca' (1); Raffaella Ferraccioli (2); Marta Catellani (1)/titolo:Unsymmetrical Aryl-Aryl Cross-Coupling Leading to 6H-Dibenzopyrans./doi:10.1055%2Fs-2007-990934/rivista:Synthesis (Stuttg.)/anno:2008/pagina_da:995/pagina_a:997/intervallo_pagine:995–997/volume:6
Publication Year :
2008
Publisher :
Thieme., Stuttgart , Germania, 2008.

Abstract

6 H-Dibenzopyrans are prepared starting from ORTHO-substituted aryl iodides, O-bromophenols and activated olefins, in the presence of a catalytic system based on palladium acetate and norbornene by means of a simple and efficient, one-pot, three-component procedure under mild conditions.

Details

Language :
English
Database :
OpenAIRE
Journal :
Synthesis (Stuttg.) 6 (2008): 995–997. doi:10.1055/s-2007-990934, info:cnr-pdr/source/autori:Elena Motti (1); Nicola Della Ca' (1); Raffaella Ferraccioli (2); Marta Catellani (1)/titolo:Unsymmetrical Aryl-Aryl Cross-Coupling Leading to 6H-Dibenzopyrans./doi:10.1055%2Fs-2007-990934/rivista:Synthesis (Stuttg.)/anno:2008/pagina_da:995/pagina_a:997/intervallo_pagine:995–997/volume:6
Accession number :
edsair.doi.dedup.....c3a353ab7df91d92de3c511dc2f2c4b0