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 multivariate factor optimisation. 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 process
Non-ionic deep eutectic solvent (ni-DES) possesses various advantages such as good solvation, biodeg...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
Conditions for the Suzuki–Miyaura coupling of lithium triisopropyl borates are reported, as well as ...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
Previously held under moratorium in Chemistry Department (GSK) from March 2016 until March 2018The c...
This Minireview gives a complete overview of the Suzuki-Miyaura coupling reaction involving aryl dia...
Stable, catalytically active palladium nanoparticles of various average diameters (1.9–7.4 nm) have ...
<p>Optimization of conditions for the Suzuki–Miyaura coupling of aryl halides with phenylboronic aci...
Pd-catalyzed Suzuki–Miyaura cross-coupling between (hetero)aryl halides (Cl, Br, I) and versatile, m...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Parallel microscale experimentation was used to develop general conditions for the Suzuki-Miyaura cr...
Non-ionic deep eutectic solvent (ni-DES) possesses various advantages such as good solvation, biodeg...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
Conditions for the Suzuki–Miyaura coupling of lithium triisopropyl borates are reported, as well as ...
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
Previously held under moratorium in Chemistry Department (GSK) from March 2016 until March 2018The c...
This Minireview gives a complete overview of the Suzuki-Miyaura coupling reaction involving aryl dia...
Stable, catalytically active palladium nanoparticles of various average diameters (1.9–7.4 nm) have ...
<p>Optimization of conditions for the Suzuki–Miyaura coupling of aryl halides with phenylboronic aci...
Pd-catalyzed Suzuki–Miyaura cross-coupling between (hetero)aryl halides (Cl, Br, I) and versatile, m...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Parallel microscale experimentation was used to develop general conditions for the Suzuki-Miyaura cr...
Non-ionic deep eutectic solvent (ni-DES) possesses various advantages such as good solvation, biodeg...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
Conditions for the Suzuki–Miyaura coupling of lithium triisopropyl borates are reported, as well as ...