Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions

Medchemcomm. 2018 May 17;9(7):1188-1193. doi: 10.1039/c8md00185e. eCollection 2018 Jul 1.

Abstract

Herein, we describe the development of copper-catalyzed cross-coupling of DNA-conjugated aryl iodides with aliphatic amines. This protocol leverages a novel ligand, 2-((2,6-dimethoxyphenyl)amino)-2-oxoacetic acid, to effect the transformation in aqueous DMSO, under mild conditions and in air, making it an ideal candidate for the synthesis of DNA-encoded libraries.