文摘
Pd-catalyzed regioselective coupling of γ-C(sp3)–H bonds of oxalyl amide-protected amino acids with heteroaryl and aryl iodides is reported. A wide variety of iodides are tolerated, giving the corresponding products in moderate to good yields. Various oxalyl amide-protected amino acids were compatible in this C–H transformation, thus representing a practical method for constructing non-natural amino acid derivatives.