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research article
Manganese-mediated reductive amidation of esters with nitroarenes
March 21, 2019
Amides are ubiquitous molecules in nature and in synthetic chemistry. Here we report a convenient and efficient method to synthesize N-aryl amides via amidation of esters with nitroarenes. In the presence of manganese metal, this amidation proceeded smoothly without the need for additional catalysts or ligands. Various esters and nitroarenes are suitable substrates to afford a wide range of N-aryl amides, including bio-active molecules and intermediates to drug molecules.
Type
research article
Web of Science ID
WOS:000462670600006
Authors
Publication date
2019-03-21
Publisher
Published in
Volume
6
Issue
6
Start page
756
End page
761
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
June 18, 2019
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