Wang, Xiao-Xia published the artcileN-Heterocyclic carbene-palladium(II)-1-methylimidazole complex-catalyzed Suzuki-Miyaura coupling of benzyl carbamates with arylboronic acids, Safety of Bis(4-fluorophenyl)methane, the publication is Organic & Biomolecular Chemistry (2015), 13(47), 11438-11444, database is CAplus and MEDLINE.
The Suzuki-Miyaura coupling of benzyl carbamates with arylboronic acids was achieved in an environmentally benign medium. Using water as the sole solvent, such transformation took place very well to give the desired diarylmethane derivatives in good to almost quant. yields in the presence of a well-defined NHC-Pd(II)-Im complex under mild conditions. It is worth noting here that this is the first example of benzyl carbamates used in the coupling reaction, thus affording a new method for the formation of diarylmethanes by palladium-catalyzed C-O bond activation.
Organic & Biomolecular Chemistry published new progress about 457-68-1. 457-68-1 belongs to catalysis-chemistry, auxiliary class Fluoride,Benzene, name is Bis(4-fluorophenyl)methane, and the molecular formula is C3H6O2, Safety of Bis(4-fluorophenyl)methane.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia