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  4. Anhydrous Conditions Enable the Catalyst-Free Carboxylation of Aromatic Alkynes with CO2 under Mild Conditions
 
research article

Anhydrous Conditions Enable the Catalyst-Free Carboxylation of Aromatic Alkynes with CO2 under Mild Conditions

Toniolo, Davide  
•
Bobbink, Felix D.  
•
Dyson, Paul J.  
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January 27, 2020
Helvetica Chimica Acta

The direct carboxylation of aromatic alkynes with CO2, a cheap and widely available C1 source, is the most attractive method for the synthesis of carboxylic acids. Here we show that direct carboxylation of terminal alkynes can be simply performed in near-quantitative yield in four hours with anhydrous Cs2CO3 under mild conditions without need of a metal catalyst.

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Type
research article
DOI
10.1002/hlca.201900258
Web of Science ID

WOS:000509411700001

Author(s)
Toniolo, Davide  
Bobbink, Felix D.  
Dyson, Paul J.  
Mazzanti, Marinella  
Date Issued

2020-01-27

Published in
Helvetica Chimica Acta
Volume

103

Issue

2

Article Number

e1900258

Subjects

Chemistry, Multidisciplinary

•

Chemistry

•

alkynes

•

carbon dioxide fixation

•

propiolic acids

•

c-h activation

•

cesium carbonate

•

carbon-dioxide

•

terminal alkynes

•

n-formylation

•

methylation

•

mechanism

•

bonds

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCOM  
SCI-SB-MM  
Available on Infoscience
March 3, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/166621
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