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 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