Description

• Application: 4-Fluorophenylboronic acid can be used as a reactant in coupling reactions with arenediazonium tetrafluoroborates,[1] iodonium salts, and iodanes.[2] It is also used to make novel biologically active terphenyls.[3]It can also be used as a reactant in: Suzuki coupling using microwave and triton B catalyst.[4] Pd-catalyzed direct arylation of pyrazoles with phenylboronic acids.[5] Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles.[6] Cu-catalyzed Petasis reactions.[7] Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.[8] Ruthenium catalyzed direct arylation.[9] Rh-catalyzed asymmetric conjugate additions.[10] Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.[11] Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.[12] Suzuki cross-coupling of tetrabromothiophene.[13]Palladium-catalyzed addition to nitriles.[14]
• Other Notes: Contains varying amounts of anhydride