scholarly journals Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives

2014 ◽  
Vol 10 ◽  
pp. 2912-2919 ◽  
Author(s):  
Fatma Belkessam ◽  
Aidene Mohand ◽  
Jean-François Soulé ◽  
Abdelhamid Elias ◽  
Henri Doucet

Conditions allowing the one pot 2,5-diheteroarylation of 2,5-dibromothiophene derivatives in the presence of palladium catalysts are reported. Using KOAc as the base, DMA as the solvent and only 0.5–2 mol % palladium catalysts, the target 2,5-diheteroarylated thiophenes were obtained in moderate to good yields and with a wide variety of heteroarenes such as thiazoles, thiophenes, furans, pyrroles, pyrazoles or isoxazoles. Moreover, sequential heteroarylation reactions allow the access to 2,5-diheteroarylated thiophenes bearing two different heteroaryl units.

2009 ◽  
Vol 11 (2) ◽  
pp. 265-268 ◽  
Author(s):  
Laura Rubio-Pérez ◽  
F. Javier Pérez-Flores ◽  
Pankaj Sharma ◽  
Luis Velasco ◽  
Armando Cabrera

ChemInform ◽  
2009 ◽  
Vol 40 (24) ◽  
Author(s):  
Laura Rubio-Perez ◽  
F. Javier Perez-Flores ◽  
Pankaj Sharma ◽  
Luis Velasco ◽  
Armando Cabrera

Synthesis ◽  
2017 ◽  
Vol 49 (23) ◽  
pp. 5149-5158
Author(s):  
Alavala Krishna Reddy ◽  
Gedu Satyanarayana

Palladium-catalyzed copper-free Sonogashira coupling of 2-bromocarbonyls is presented. This method afforded the 2-alkynylaryl carbonyls, useful synthons for the accomplishment of many carbocyclic and heterocyclic motifs. Significantly, the strategy was extended to the one-pot synthesis of isobenzofurans via reduction followed by intramolecular 5-exo-dig cyclization.


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