The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction was investigated from a process chemistry perspective including safety evaluation, solvent and catalyst screening and multi-variate factor optimization. Optimised conditions were applied to a range of substrates to evaluate the scope and limitations of the reaction and one example was carried out on mole-scale to demonstrate the practicality and scalability of the proces
The use of palladium nanoparticles stabilized by natural. beads made of an alginate/gellan mixture i...
The novel cationic palladium–allyl complex [Pd(C3H5)(1-(2-(methylthio)ethyl)-4-phenyl-1H-1,2,3- tria...
WOS: 000225241500011Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and cha...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki–Miyaura reaction...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction...
This Minireview gives a complete overview of the Suzuki-Miyaura coupling reaction involving aryl dia...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
Parallel microscale experimentation was used to develop general conditions for the Suzuki-Miyaura cr...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
The use of palladium nanoparticles stabilized by natural beads made of an alginate/gellan mixture in...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
Elevated pressure (15 kbar) in the liquid phase improves yields and permits the use of cheaper Fe(II...
Suzuki-Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal catalysed ca...
The use of palladium nanoparticles stabilized by natural. beads made of an alginate/gellan mixture i...
The novel cationic palladium–allyl complex [Pd(C3H5)(1-(2-(methylthio)ethyl)-4-phenyl-1H-1,2,3- tria...
WOS: 000225241500011Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and cha...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki–Miyaura reaction...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction...
This Minireview gives a complete overview of the Suzuki-Miyaura coupling reaction involving aryl dia...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
Parallel microscale experimentation was used to develop general conditions for the Suzuki-Miyaura cr...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
The use of palladium nanoparticles stabilized by natural beads made of an alginate/gellan mixture in...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
Elevated pressure (15 kbar) in the liquid phase improves yields and permits the use of cheaper Fe(II...
Suzuki-Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal catalysed ca...
The use of palladium nanoparticles stabilized by natural. beads made of an alginate/gellan mixture i...
The novel cationic palladium–allyl complex [Pd(C3H5)(1-(2-(methylthio)ethyl)-4-phenyl-1H-1,2,3- tria...
WOS: 000225241500011Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and cha...