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.s003
https://acs.figshare.com/articles/journal_contribution/Novel_Acetoxylation_and_C_C_Coupling_Reactions_at_Unactivated_Positions_in_Amino_Acid_Derivatives/3070054
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