5171-64-2

Upstream product

• 99-91-2 para-chloroacetophenone 
• 279216-31-8 C₂₄H₁₉BO 

Downstream Products

• 102147-16-0 2,4-Diphenyl-6-[1,1';4',1'']terphenyl-4-yl-nicotinonitrile 
• 102147-19-3 2-Biphenyl-4-yl-4-phenyl-6-[1,1';4',1'']terphenyl-4-yl-nicotinonitrile 
• 5731-15-7 [1,1':4',1''-terphenyl]-4-carboxylic acid 
• 104416-16-2 2-benzylidene-3-(4-p-terphenylyl)-3-oxopropanenitrile 
• 104416-17-3 3,5-dicyano-4-phenyl-2,6-bis(4-p-terphenylyl)-1,4-dihydropyridine 
• 104416-18-4 3,5-dicyano-4-phenyl-2,6-bis(4-p-terphenylyl)pyridine 

Relevant academic research and scientific papers

Palladium-catalyzed cross-coupling reaction of potassium diaryldifluoroborates with aryl halides

The catalytic cross-coupling reaction of potassium diaryldifluoroborates with aryl halides proceeds to afford the biphenyls in good yields. These salts on an arylation reagent were readily prepared via a protocol of the Grignard method and transformation to potassium salts. Two aryl groups of these salts were efficiently transferred in the Suzuki-Miyaura reaction.