Description
Application
4-(Trifluoromethyl)phenylboronic acid can be used as a reactant in:
Site-selective Suzuki-Miyaura cross-coupling reactions.
Palladium-catalyzed direct arylation reactions.
Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.
Ruthenium catalyzed direct arylation.
Ligand-free copper-catalyzed coupling reactions.
Amination and conjugate addition reactions.
Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.
Rhodium-catalyzed asymmetric 1,4-addition reactions.
Copper-catalyzed nitration reactions.
Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.
Palladium catalyzed allylation reaction with allyl alcohols.
N-Arylation of imidazoles and amines in the presence of copper-exchanged fluorapatite as a catalyst.
It can also be used as a reactant to prepare:
Thiazole derivatives for printable electronics.
Terphenyl benzimidazoles as tubulin polymerization inhibitors.
Aryl ketones by cross-coupling reaction with acid chlorides.
Other Notes
Contains varying amounts of anhydride