The palladium catalyzed alkynylation of aryl halides (Sonogashira reaction) has been achieved in pure water without any additives or phase transfer catalysts. The reaction, which requires only 0.5mol% of $Pd(PPh_3)_4$ catalyst, is remarkably fast (30min at $70^oC$) producing high yields of the aryl alkyne products
The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environm...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
The palladium catalyzed alkynylation of aryl halides (Sonogashira reaction) has been achieved in pur...
The Pd-catalyzed alkynylation of various alkenyl halides and triflates with alkynylzincs proceeds we...
We report the synthesis of 2-(3-sulfonatomesityl)-5-sulfonatoindenyl(dicyclohexylphosphine hydrate s...
A heterogeneous catalyst, nanosized MCM-41-Pd, was used to catalyze the Sonogashira coupling of aryl...
A mild protocol for the copper-free Sonogashira coupling of aryl iodides with terminal acetylenes in...
Sonogashira reaction and oxidative dimerisation of terminal alkynes are among the most relevant and ...
<div><p></p><p>Glycine, as a kind of commercially available and inexpensive ligand, is used to prepa...
Palladium-catalyzed Heck alkynylation cross-coupling reactions between terminal alkynes and deactiva...
Unsymmetrical diarylalkynes have attracted much atten-tion, as the molecule structure, having an int...
Triarylsulfonium, alkyl- and fluoroalkyl(diaryl)sulfonium, and aryl(dialkyl)sulfonium triflates ...
A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Son...
A series of inorganic and organometallic compounds of gold [AuCl(tht)], [Au(C6F5)(tht)] and Na[AuCl4...
The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environm...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
The palladium catalyzed alkynylation of aryl halides (Sonogashira reaction) has been achieved in pur...
The Pd-catalyzed alkynylation of various alkenyl halides and triflates with alkynylzincs proceeds we...
We report the synthesis of 2-(3-sulfonatomesityl)-5-sulfonatoindenyl(dicyclohexylphosphine hydrate s...
A heterogeneous catalyst, nanosized MCM-41-Pd, was used to catalyze the Sonogashira coupling of aryl...
A mild protocol for the copper-free Sonogashira coupling of aryl iodides with terminal acetylenes in...
Sonogashira reaction and oxidative dimerisation of terminal alkynes are among the most relevant and ...
<div><p></p><p>Glycine, as a kind of commercially available and inexpensive ligand, is used to prepa...
Palladium-catalyzed Heck alkynylation cross-coupling reactions between terminal alkynes and deactiva...
Unsymmetrical diarylalkynes have attracted much atten-tion, as the molecule structure, having an int...
Triarylsulfonium, alkyl- and fluoroalkyl(diaryl)sulfonium, and aryl(dialkyl)sulfonium triflates ...
A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Son...
A series of inorganic and organometallic compounds of gold [AuCl(tht)], [Au(C6F5)(tht)] and Na[AuCl4...
The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environm...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...