Kawase, Misa published the artcileSuzuki-Miyaura Cross-Coupling Reaction with Potassium Aryltrifluoroborate in Pure Water Using Recyclable Nanoparticle Catalyst, Product Details of C14H14, the publication is Synlett (2022), 33(1), 57-61, database is CAplus.
The Suzuki-Miyaura cross-coupling reaction of aryl bromides with potassium aryltrifluoroborates in water catalyzed by linear polystyrene-stabilized PdO nanoparticles (PS-PdONPs) was described to obtain biaryls Ar1Ar2 [Ar1 = Ph, 2-MeC6H4, 3-furyl, etc.; Ar2 = 2-MeC6H4, 4-MeC6H4, 4-MeOC6H4, 4-F3CC6H4, 4-AcC6H4]. The reaction of aryl bromides having electron-withdrawing groups or electron-donating groups took place smoothly to give the corresponding coupling product in high yields. The catalyst recycles five times without significant loss of catalytic activity although a little bit increase in size of PdNPs was observed after the reaction.
Synlett published new progress about 613-33-2. 613-33-2 belongs to catalysis-chemistry, auxiliary class Benzene, name is 4,4′-Dimethyldiphenyl, and the molecular formula is C14H14, Product Details of C14H14.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia