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  4. Manganese-mediated reductive amidation of esters with nitroarenes
 
research article

Manganese-mediated reductive amidation of esters with nitroarenes

Cheung, Chi Wai  
•
Shen, Ni  
•
Wang, Shao-Peng
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March 21, 2019
Organic Chemistry Frontiers

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.

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Type
research article
DOI
10.1039/c8qo01405a
Web of Science ID

WOS:000462670600006

Author(s)
Cheung, Chi Wai  
Shen, Ni  
Wang, Shao-Peng
Ullah, Asim
Hu, Xile  
Ma, Jun-An
Date Issued

2019-03-21

Publisher

ROYAL SOC CHEMISTRY

Published in
Organic Chemistry Frontiers
Volume

6

Issue

6

Start page

756

End page

761

Subjects

Chemistry, Organic

•

Chemistry

•

amide bond formation

•

peptide coupling reagents

•

secondary amides

•

carboxylic-acids

•

transamidation

•

metal

•

hydroamination

•

activation

•

amines

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
UPSCHOONJANS  
Available on Infoscience
June 18, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/157078
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