Novel Acetoxylation and C−C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives
journal contributionposted on 20.07.2006 by B. V. Subba Reddy, Leleti Rajender Reddy, E. J. Corey
Any type of content formally published in an academic journal, usually following a peer-review process.
Under special conditions, N-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.