A simple and efficient recyclable phosphine-free catalytic system for alkoxycarbonylation and carbonylative Sonogashira coupling reactions of aryl iodides

2008 ◽  
Vol 253 (1) ◽  
pp. 50-56 ◽  
Author(s):  
J LIU ◽  
J CHEN ◽  
C XIA
2019 ◽  
Vol 43 (9-10) ◽  
pp. 431-436
Author(s):  
Fatemeh Rezaeimanesh ◽  
Mohammad Bakherad ◽  
Hossein Nasr-Isfahani

An efficient method is developed for the synthesis of 4-(3-arylprop-2-ynyloxy)-6-methyl-2-(methylthio)pyrimidines via palladium-catalyzed Sonogashira reactions of 4-methyl-2-(methylthio)-6-(prop-2-yn-1-yloxy)pyrimidine with electron-poor aryl iodides in acetonitrile at room temperature. Excellent yields of the products were obtained in reaction times of 9–11 h.


2018 ◽  
Vol 7 (6) ◽  
pp. 1113-1117 ◽  
Author(s):  
Ancheng Shen ◽  
Zhen Wu ◽  
Yue Fang ◽  
Jinming Yang ◽  
Haibo Zhu ◽  
...  

2012 ◽  
Vol 53 (28) ◽  
pp. 3556-3559 ◽  
Author(s):  
Marcio S. Silva ◽  
Renan S. Ferrarini ◽  
Bruno A. Sousa ◽  
Fabiano T. Toledo ◽  
João V. Comasseto ◽  
...  

2015 ◽  
Vol 11 ◽  
pp. 2297-2305 ◽  
Author(s):  
Svetlana Petrovna Panchenko ◽  
Alexei Dmitrievich Averin ◽  
Maksim Viktorovich Anokhin ◽  
Olga Aleksandrovna Maloshitskaya ◽  
Irina Petrovna Beletskaya

The Cu(I)-catalyzed N,N’-diarylation of natural diamines and polyamines such as putrescine, cadaverine, spermine, spermidine and their homologues is described. Aryl iodides bearing electron-donating and electron-withdrawing groups have been employed in the study. The CuI/2-(isobutyryl)cyclohexanone/DMF catalytic system has found to be more efficient in the diarylation of diamines and spermine while the CuI/L-proline/EtCN system proved to be preferable for the diarylation of other tri- and tetraamines like spermidine, norspermidine and norspermine.


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