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Data for Synthesis of enantiomerically-enriched N-aryl amino-amides via Jocic-type reaction Christian Hobson (12004538) Michael S. Perryman (24845038) Gavin Kirby (24898684) Guy J. Clarkson (1301127) David J. Fox (1909222) Chemical reactions Aromatic amines Enantiomers Migrated from ePrints 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.<br><br>--> File types: PDF files, .par files, .dat files --> Organisation: Files organised into substances analysed in main article, which contain information detailing the substances under set HPLC, IR, NMR and Mass Spec conditions. Contains PDFs showing graphs and other files containing the raw data underpinning figures. 2018-04-16T00:00:00Z Dataset Dataset 10.82444/warw.33755380.v1 https://figshare.com/articles/dataset/Data_for_Synthesis_of_enantiomerically-enriched_N-aryl_amino-amides_via_Jocic-type_reaction/33755380 CC BY 4.0