Palladium-catalyzed β-C(sp3)-H arylation of phthaloyl alanine with hindered aryl iodides: synthesis of complex β-aryl α-amino acids

An efficient protocol for palladium-catalyzed beta-C(sp(3))-H arylation of aliphatic carboxamides equipped with a 2-(2-pyridyl) ethylamine (PE) auxiliary was developed. The PE auxiliary is uniquely effective at facilitating the arylation of primary C(sp(3))-H bonds with sterically hindered aryl iodides. A variety of aryl iodides bearing alkoxyl, carbonyl, nitro and halogen groups on the ortho position can react with the PE-coupled phthaloyl alanine substrate in moderate to excellent yield. These reactions offer a useful solution for preparing complex beta-aryl alpha-amino acid products from readily accessible starting materials.