Novel Acetoxylation and C−C Coupling
Reactions at Unactivated Positions in
α-Amino Acid Derivatives

V. Subba Reddy, B.; Reddy, Leleti Rajender; Corey, E. J.

doi:10.1021/ol061389j.s003

Novel Acetoxylation and C−C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives

https://doi.org/10.1021/ol061389j.s003
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journal contribution

posted on 2006-07-20, 00:00 authored by B. V. Subba Reddy, Leleti Rajender Reddy, E. J. Corey

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.

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Keywords

acetoxylated aminoquinoline DerivativesUnder acid arylated Unactivated Positions arylation amide Novel Acetoxylation Amino

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