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Data for Synthesis of enantiomerically-enriched N-aryl amino-amides via Jocic-type reaction
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Hobson, Christian, Perryman, Michael S., Kirby, Gavin, Clarkson, Guy J. and Fox, David J. (2018) Data for Synthesis of enantiomerically-enriched N-aryl amino-amides via Jocic-type reaction. [Dataset]
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N-Aryl data.zip - Published Version Available under License Creative Commons Attribution 4.0. Download (55Mb) |
Official URL: https://wrap.warwick.ac.uk/101137/
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.
Item Type: | Dataset | ||||||
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Subjects: | Q Science > QD Chemistry | ||||||
Divisions: | Faculty of Science, Engineering and Medicine > Science > Chemistry | ||||||
Type of Data: | Experimental data | ||||||
Library of Congress Subject Headings (LCSH): | Chemical reactions, Aromatic amines, Enantiomers | ||||||
Publisher: | University of Warwick, Department of Chemistry | ||||||
Official Date: | 16 April 2018 | ||||||
Dates: |
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Status: | Not Peer Reviewed | ||||||
Publication Status: | Published | ||||||
Media of Output (format): | .pdf .par .dat | ||||||
Access rights to Published version: | Open Access (Creative Commons) | ||||||
Copyright Holders: | University of Warwick | ||||||
Description: | --> File types: |
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Date of first compliant deposit: | 2 March 2020 | ||||||
Date of first compliant Open Access: | 2 March 2020 | ||||||
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