Amide synthesis via nickel-catalysed reductive aminocarbonylation of aryl halides with nitroarenes
Author:
Affiliation:
1. Laboratory of Inorganic Synthesis and Catalysis
2. Institute of Chemical Sciences and Engineering
3. Ecole Polytechnique Fédérale de Lausanne (EPFL)
4. ISIC-LSCI
5. Lausanne 1015
Abstract
A nickel-catalysed reductive aminocarbonylation of (hetero)aryl halides employing readily available nitro(hetero)arenes as the nitrogen source has been developed.
Funder
École Polytechnique Fédérale de Lausanne
H2020 Marie Skłodowska-Curie Actions
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/SC/C7SC03950F
Reference38 articles.
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4. Nonclassical Routes for Amide Bond Formation
5. Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals
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