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Synthesis of enantiomerically-enriched N-aryl amino-amides via a Jocic-type reaction
Authors:Christian Hobson  Michael S. Perryman  Gavin Kirby  Guy J. Clarkson  David J. Fox
Affiliation:Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK
Abstract:Enantiomerically-enriched secondary trichloromethyl-alcohols react with aryl amines to give enantiomerically-enriched α-N-arylamino-acid derivatives. The intermediate acid chlorides can react in situ with aryl or, regioselectively, with alkyl amines to give aryl or alkyl α-N-arylamino amides.
Keywords:Jocic reaction  Enantiomerically-enriched
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