The palladium-catalysed coupling of aryl halides with terminal alkynes can be performed using base, zinc chloride and sodium iodide. This protocol represents a convenient method for the generation of nucleophilic acetylides in situ.Geoffrey T Crisp, Peter D Turner, Kim A Stephen
A completely atom economical palladium‐catalyzed addition reaction has been developed to stereoselec...
actions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearin...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
Palladium(II)-catalyzed coupling of terminal alkynes with unactivated aryl iodides occurs at room te...
Palladium-catalysed coupling reactions have gained importance as a tool for the production of pharma...
We report a new class of catalytic reaction: the thermal substitution of a secondary and or tertiary...
The first part of this thesis discusses an unprecedented acylation of allylic mercurials by acyl chl...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
Organolithium compounds are amongst the most important organometallic reagents and frequently used i...
Two efficient protocols for the palladium-catalyzed synthesis of aryl-2-methyl-3-butyn-2-ols from ar...
The catalyst precursor consisting of a mixt. of 10% palladium on carbon and 3.9 equiv. of AsPh3 as w...
A straightforward methodology for the decarboxylative cross-coupling of aryl bromides and phenylprop...
Pd catalyzed cross coupling reactions are extensively used to effect a multitude of organic transfor...
Through a salt metathesis reaction, ( t-BuPCN)Pd-ONO2 (2) was prepared and used as a precursor for p...
The incorporation of alkynes into organic molecules is one of the most valuable transformations for ...
A completely atom economical palladium‐catalyzed addition reaction has been developed to stereoselec...
actions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearin...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
Palladium(II)-catalyzed coupling of terminal alkynes with unactivated aryl iodides occurs at room te...
Palladium-catalysed coupling reactions have gained importance as a tool for the production of pharma...
We report a new class of catalytic reaction: the thermal substitution of a secondary and or tertiary...
The first part of this thesis discusses an unprecedented acylation of allylic mercurials by acyl chl...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
Organolithium compounds are amongst the most important organometallic reagents and frequently used i...
Two efficient protocols for the palladium-catalyzed synthesis of aryl-2-methyl-3-butyn-2-ols from ar...
The catalyst precursor consisting of a mixt. of 10% palladium on carbon and 3.9 equiv. of AsPh3 as w...
A straightforward methodology for the decarboxylative cross-coupling of aryl bromides and phenylprop...
Pd catalyzed cross coupling reactions are extensively used to effect a multitude of organic transfor...
Through a salt metathesis reaction, ( t-BuPCN)Pd-ONO2 (2) was prepared and used as a precursor for p...
The incorporation of alkynes into organic molecules is one of the most valuable transformations for ...
A completely atom economical palladium‐catalyzed addition reaction has been developed to stereoselec...
actions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearin...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...