297163-75-8

Upstream product

• 135273-60-8 (dichloro)(ethyl)(4-methylphenyl)silane 

Downstream Products

• 53040-92-9 4-(4-tolyl)anisole 
• 42353-96-8 1-methyl-4-[(1E)-1-propyl-1-penten-1-yl]benzene 
• 34909-37-0 (E)-N,N-dimethyl-3-(p-tolyl)acrylamide 
• 123248-21-5 (E)-n-butyl 3-(p-tolyl)acrylate 
• 7774-79-0 4-(4-methylphenyl)butan-2-one 
• 56955-36-3 methyl 3-(p-tolyl)propionate 
• 20754-20-5 3-p-tolyl-acrylic acid methyl ester 
• 29417-79-6 methyl 2-methyl-3-(4-methylphenyl)propanoate 
• 3160-38-1 (E)-4-p-tolylbut-3-en-2-one 
• 97585-04-1 ethyl (E)-3-(4-methylphenyl)acrylate 
• 7116-41-8 ethyl 3-(4-methylphenyl)propanoate 
• 136053-53-7 tert-butyl 4-methylcinnamate 
• 379218-64-1 tert-butyl 3-(4-methylphenyl)propanoate 

Relevant academic research and scientific papers

Palladium-Catalyzed Cross-Coupling of Silanols, Silanediols, and Silanetriols Promoted by Silver(I) Oxide

Palladium-catalyzed cross-coupling of aryl- or alkenylsilanols, silanediols, and silanetriols with a variety of iodoarenes by the catalysis of palladium(0) and in the presence of silver(I) oxide furnished the coupling products in good to excellent yields. The reactions of silanediols or silanetriols under similar conditions proceeded much faster than those of silanols to afford the corresponding coupling products in excellent yields within shorter reaction periods (5-12 h). The measurement of the X-ray diffraction (XRD) pattern of the silver residue after the reaction revealed that silver(I) oxide was converted to silver(I) iodide.