Novel Acetoxylation and C−C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives B. V. Subba Reddy Leleti Rajender Reddy E. J. Corey 10.1021/ol061389j.s004 https://acs.figshare.com/articles/journal_contribution/Novel_Acetoxylation_and_C_C_Coupling_Reactions_at_Unactivated_Positions_in_Amino_Acid_Derivatives/3070051 Under special conditions, <i>N</i>-phthaloyl-α-amino acid amides of 8-aminoquinoline can be either acetoxylated or arylated selectively at the β-carbon. In certain cases, arylation can be effected at the γ-carbon. 2006-07-20 00:00:00 acetoxylated aminoquinoline DerivativesUnder acid arylated Unactivated Positions arylation amide Novel Acetoxylation Amino