25882-27-3

Upstream product

• 100-66-3 methoxybenzene 
• 108-55-4 glutaric anhydride, 
• 150075-20-0 1-(4-methoxyphenyl)pentane-1,5-diol 
• 64-17-5 ethanol 
• 154477-03-9 5-(4'-methoxyphenyl)-4-pentyn-1-ol 
• 25305-58-2 ethyl 5-(4-methoxyphenyl)-5-oxopentanoate 
• 136538-25-5 1-<2-(5,6-Dihydro-4H-pyranyl)>-4,4-dimethoxy-2,5-cyclohexadien-1-ol 

Downstream Products

• 25882-26-2 4-p-Anisoylbutyl-toluol-p-sulfonat 
• 387358-62-5 5-(4-methoxyphenyl)-5-oxo-pentanal 
• 1396203-26-1 ethyl 2-((2R,6S)-6-(4-methoxyphenyl)tetrahydro-2H-pyran-2-yl)acetate 
• 1396203-22-7 ethyl 7-hydroxy-7-(4-methoxyphenyl)heptanoate 
• 31526-43-9 5-ethoxy-1-(4-methoxyphenyl)pentan-1-one 

Relevant academic research and scientific papers

Controlling Chemoselectivity of Catalytic Hydroboration with Light

The ability to selectively react one functional group in the presence of another underpins efficient reaction sequences. Despite many designer catalytic systems being reported for hydroboration reactions, which allow introduction of a functional handle fo

Mpg-C3N4-catalyzed selective oxidation of alcohols using O2 and visible light

Mesoporous carbon nitride (mpg-C3N4) polymer can function as a metal-free photocatalyst to activate O2 for the selective oxidation of benzyl alcohols with visible light, avoiding the cost, toxicity, and purification problems associated with corresponding transition-metal systems. By combining the surface basicity and semiconductor functions of mpg-C3N4, the photocatalytic system can realize a high catalytic selectivity to generate benzaldehyde. The metal-free photocatalytic system also selectively converts other alcohol substrates to their corresponding aldehydes/ketones, demonstrating a potential pathway of accessing traditional mild radical chemistry with nitroxyl radicals.

p-Toluenesulfonic acid-promoted selective functionalization of unsymmetrical arylalkynes: a regioselective access to various arylketones and heterocycles

Regioselective hydration of a wide range of internal alkynes has been afforded in high to good yields by using PTSA in EtOH. The scope of the reaction of alkynes has been delineated. Arylaliphatic alkynes and diarylalkynes were regioselectively hydrated in good to excellent yields and short reaction times when the reaction was achieved under microwave irradiation. Moreover, diarylalkynes, arylenynes as well as diaryldiynes bearing a methoxy- or a thiomethyl substituent on the ortho position underwent a regioselective 5-endo-dig-cyclization to give a variety of 2-aryl- and 2-styrylbenzofuran or benzothiphene derivatives. We believe that, this new environmentally metal-free procedure combined to microwave irradiation would be in importance in the search of green laboratory-scale synthesis.