Description

• Application: 4-(Trifluoromethyl)phenylboronic acid can be used as a reactant in:Site-selective Suzuki-Miyaura cross-coupling reactions.[1]Palladium-catalyzed direct arylation reactions.[2]Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.[3]Ruthenium catalyzed direct arylation.[4]Ligand-free copper-catalyzed coupling reactions.[5]Amination and conjugate addition reactions.[6]Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.[7]Rhodium-catalyzed asymmetric 1,4-addition reactions.[8]Copper-catalyzed nitration reactions.[9]Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.[10]Palladium catalyzed allylation reaction with allyl alcohols.[11]N-Arylation of imidazoles and amines in the presence of copper-exchanged fluorapatite as a catalyst.[12]It can also be used as a reactant to prepare:Thiazole derivatives for printable electronics.[13]Terphenyl benzimidazoles as tubulin polymerization inhibitors.[14] Aryl ketones by cross-coupling reaction with acid chlorides.[15]
• Other Notes: Contains varying amounts of anhydride