This work reports the carbonylative Suzuki–Miyaura coupling of aryl iodides catalyzed by palladacycles. More importantly, the palladacycles have been used to generate high turnover numbers (TON’s) and turnover frequencies (TOF’s). A range of aryl iodides can be coupled with arylboronic acids, generating TON’s in the range of 10<sup>6</sup> to 10<sup>7</sup> and TOF’s in the range of 10<sup>5</sup> to 10<sup>6</sup> h<sup>–1</sup>. Comparison of the palladacycles with a conventional palladium source shows their superiority in generating high TON’s and TOF’s
Silica modified with organic dicationic moieties proved to be an excellent support for palladium cat...
The Pd/CeO2 system behaves as an efficient precatalyst for the Suzuki–Miyaura cross-coupling under m...
Highly selective carbonylative Suzuki reactions of aryl iodides with arylboronic acids using an in s...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
We have explored fundamental Pd-catalyzed Csp2− Csp2 Suzuki−Miyaura cross-couplings of aryl iodides ...
Palladium-catalysed coupling reactions have gained importance as a tool for the production of pharma...
Bis(thiazole) pincer palladium complexes showed efficient catalytic activity for the Suzuki–Miyaura...
We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of a...
A mechanism, which is distinct from the traditional one when sodium alkoxide was used instead of ter...
We have explored fundamental Pd-catalyzed C<sub>sp<sup>2</sup></sub>–C<sub>sp<sup>2</sup></sub> Suzu...
We present a type of palladacyclic complexes derived from arylphosphinamides which can be used as ef...
A palladium-catalyzed domino Heck cyclization/carbonylative Hiyama–Denmark cross-coupling reaction b...
The reaction between the equimolar amounts of <i>cis</i>-[PdCl<sub>2</sub>(CNR<sup>1</sup>)<sub>2</s...
The SiliaCat Pd(0) solid catalyst can be efficiently employed in the Suzuki–Miyaura cross-coupling o...
[a]<p><i>Reaction conditions:</i> aryl halide (0.6 mmol), phenylboronic acid (0.7 mmol), TBAB (1 mmo...
Silica modified with organic dicationic moieties proved to be an excellent support for palladium cat...
The Pd/CeO2 system behaves as an efficient precatalyst for the Suzuki–Miyaura cross-coupling under m...
Highly selective carbonylative Suzuki reactions of aryl iodides with arylboronic acids using an in s...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
We have explored fundamental Pd-catalyzed Csp2− Csp2 Suzuki−Miyaura cross-couplings of aryl iodides ...
Palladium-catalysed coupling reactions have gained importance as a tool for the production of pharma...
Bis(thiazole) pincer palladium complexes showed efficient catalytic activity for the Suzuki–Miyaura...
We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of a...
A mechanism, which is distinct from the traditional one when sodium alkoxide was used instead of ter...
We have explored fundamental Pd-catalyzed C<sub>sp<sup>2</sup></sub>–C<sub>sp<sup>2</sup></sub> Suzu...
We present a type of palladacyclic complexes derived from arylphosphinamides which can be used as ef...
A palladium-catalyzed domino Heck cyclization/carbonylative Hiyama–Denmark cross-coupling reaction b...
The reaction between the equimolar amounts of <i>cis</i>-[PdCl<sub>2</sub>(CNR<sup>1</sup>)<sub>2</s...
The SiliaCat Pd(0) solid catalyst can be efficiently employed in the Suzuki–Miyaura cross-coupling o...
[a]<p><i>Reaction conditions:</i> aryl halide (0.6 mmol), phenylboronic acid (0.7 mmol), TBAB (1 mmo...
Silica modified with organic dicationic moieties proved to be an excellent support for palladium cat...
The Pd/CeO2 system behaves as an efficient precatalyst for the Suzuki–Miyaura cross-coupling under m...
Highly selective carbonylative Suzuki reactions of aryl iodides with arylboronic acids using an in s...