93131-73-8

Upstream product

• 106-44-5 p-cresol 
• 375-72-4 Nonafluorobutanesulfonyl fluoride 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 98-80-6 phenylboronic acid 

Downstream Products

• 5405-15-2 N-benzyl-N-(4-methylphenyl)amine 
• 104-85-8 para-methylbenzonitrile 
• 30015-86-2 3-(4-methylphenyl)-1H-indole 
• 167283-32-1 N-(p-tolyl)indole 
• 1151856-26-6 3-methyl-3-(p-tolyl)-indoline 
• 26926-25-0 ethyl (4-methylphenyl)phenylphosphinate 
• 1754-46-7 diethyl 4-methylphenylphosphonate 
• 55008-95-2 (4-methylphenyl)di(n-butyl)phosphine oxide 
• 797-70-6 tri(4-methylphenyl)phosphine oxide 
• 6840-28-4 diphenyl(p-tolyl)phosphine oxide 
• 122334-36-5 N-methoxy-N,4-dimethylbenzamide 
• 599-86-0 4-methyl-N-(4-methylphenyl)benzenesulfonamide 
• 16803-95-5 4-(4-tolylaminosulfonyl)aniline 
• 1286478-99-6 N-(p-tolyl)-4-(trifluoromethyl)benzenesulfonamide 

Relevant academic research and scientific papers

Palladium-catalyzed one-pot cross-coupling of phenols using nonafluorobutanesulfonyl fluoride

Palladium-catalyzed coupling reactions, such as the Suzuki-Miyaura, Sonogashira, Stille, and Buchwald-Hartwig couplings, of phenols using nonafluorobutanesulfonyl fluoride (NfF) are described. These reactions proceeded through the in situ nonaflation of p