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Table · dataset · 2018

Data for Synthesis of enantiomerically-enriched N-aryl amino-amides via Jocic-type reaction

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Enantiomerically-enriched secondary trichloromethyl-alcohols react with aryl amines to give enantiomerically-enriched α-N-arylamino-acid derivatives.

Description

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.

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Organic chemistry 70%
Provenance · 1 source records, 17 field assertions
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