Aryl Iodides in Suzuki Cross-Coupling Reactions

Author(s):  
D. A. Black ◽  
K. Fagnou
Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3292 ◽  
Author(s):  
Kazuki Komoda ◽  
Rei Iwamoto ◽  
Masakazu Kasumi ◽  
Hideki Amii

A convenient and effective route for the synthesis of aryl(difluoromethyl)phosphonates has been developed based on cross-coupling reactions. Upon treatment with a stoichiometric amount (or a catalytic amount in some cases) of CuI and CsF, aryl iodides reacted smoothly with (silyldifluoromethyl)phosphonates to give the corresponding aryl(difluoromethyl)phosphonates in good yields.


2011 ◽  
Vol 13 (5) ◽  
pp. 1218-1221 ◽  
Author(s):  
Amruta Joshi-Pangu ◽  
Madhu Ganesh ◽  
Mark R. Biscoe

RSC Advances ◽  
2016 ◽  
Vol 6 (111) ◽  
pp. 109296-109300 ◽  
Author(s):  
Xian Wang ◽  
Zhenhua Wang ◽  
Zunyuan Xie ◽  
Guofang Zhang ◽  
Weiqiang Zhang ◽  
...  

1,3-Yones as σ-, π-electron donating ligands significantly accelerated the cross-coupling reactions of aryl iodides with terminal alkynes, in which as low as 0.1 to 1 mol% of CuI were efficiently activated.


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