Asymmetric synthesis of α-aminoamides by Pd-catalyzed double carbohydroamination

Literature Information

Publication Date 2003-08-19
DOI 10.1039/B306879J
Impact Factor 6.222
Authors

Perli Nanayakkara, Howard Alper


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Abstract

Tris(dibenzylideneacetone)dipalladium(0) [Pd2(dba)3] catalyzed asymmetric double carbohydroamination of iodoarenes in the presence of a chiral ligand (Trost ligand and Me-DuPHOS are most effective) is an excellent method for the chiral synthesis of α-aminoamides in up to 99% ee.

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