73178-09-3

Upstream product

• 624-38-4 para-diiodobenzene 
• 73177-97-6 -o-toluene 
• 27126-76-7 [hydroxy(tosyloxy)iodo]benzene 

Downstream Products

• 91228-76-1 (p-iodophenyl)(5-methyl-2-thienyl)iodonium tosylate 
• 624-38-4 para-diiodobenzene 
• 85925-63-9 p-iodophenyl(2-furyl)iodonium tosylate 
• 85925-32-2 Toluene-4-sulfonate(4-iodo-phenyl)-(5-trimethylsilanyl-furan-2-yl)-iodonium; 
• 1375917-64-8 (4-iodophenyl)(2-thienyl)iodonium tosylate 
• 1375917-62-6 (4-iodophenyl)(4-methoxyphenyl)iodonium tosylate 
• 1375917-72-8 (4-iodophenyl)(4-methoxyphenyl)iodonium bromide 
• 1375917-67-1 (4-iodophenyl)(4-methoxyphenyl)iodonium triflate 
• 1375917-69-3 (4-iodophenyl)(2-thienyl)iodonium triflate 
• 1428552-13-9 (2,2-dimethyl-5,7-dioxo-1,3-dioxocan-6-yl)-(4-iodophenyl)iodonium ylide 

Relevant academic research and scientific papers

Convenient preparation of (4-iodophenyl)aryliodonium salts

The (4-iodophenyl)aryliodonium salts bis(4-iodophenyl)iodonium, (4-iodophenyl)(4-methoxy-phenyl)iodonium and (4-iodophenyl)(2-thienyl)iodonium, each with three different anions, were prepared using 4-iodo-1- [hydroxy(tosyloxy)iodo]benzene. These are suita

benzene, a Versatile Reagent for the Mild Oxidation of Aryl Iodides at the Iodine Atom by Ligand Transfer

Treatment of a variety of aryl iodides with benzene (1) under mild conditions resulted in ligand transfer, and new arenes were obtained.However, with some substrates containing proximate functional groups cyclic iodonium salts and iodinanes resulted.The reaction between 1 and 2-iodothiophene took a distinctly different course.