Synfacts 2006(7): 0712-0712  
DOI: 10.1055/s-2006-941884
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York

Cu-Promoted Coupling of Imines, Acid Chlorides and Organoindium Reagents

Contributor(s): Paul Knochel, Andrei Gavryushin
D. A. Black, B. A. Arndtsen*
McGill University, Montréal, Canada
Further Information

Publication History

Publication Date:
22 June 2006 (online)

Significance

This is a new useful three-component reaction, leading directly, with a broad diversity, to interesting polyfunctionalized amides. The use of organoindium compounds allows an excellent tolerance of functional groups, which is important in the synthesis of complex biologically active compounds. A very broad range of substrates can be involved in the reaction: alkyl- and arylimines, alkyl-, vinyl- and arylindium compounds react equally well. The use of α,β-unsaturated imines leads exclusively to 1,4-addition products.