98055-01-7

Upstream product

• 147251-92-1 1-phenylsulfonyl-3-phenylthioindol-2-ylmethanol 
• 122-52-1 triethyl phosphite 
• 85678-42-8 2-(bromomethyl)-3-(phenylthio)-1-(phenylsulfonyl)-1H-indole 
• 868081-88-3 1-phenylsulfonyl-3-phenylthio-2-chloromethylindole 

Downstream Products

• 98055-10-8 1-Benzenesulfonyl-2-(3-pyridylethyl)-indole 
• 98055-09-5 2-[2-(3,4,5-Trimethoxy-phenyl)-ethyl]-1H-indole 
• 98055-06-2 2-(2-phenylethyl)-1H-indole 
• 156749-36-9 5,6-Dimethoxy-3'-phenylsulfanyl-1H,1'H-[2,2']biindolyl 
• 156749-37-0 6-(3-Phenylsulfanyl-1H-indol-2-yl)-5H-[1,3]dioxolo[4,5-f]indole 
• 226947-44-0 N-(1-benzenesulfonylindol-2-methylene)-4-(N',N'-dimethylamino)aniline 
• 226947-45-1 N-(1-benzenesulfonylindol-2-methylene)aniline 
• 98055-02-8 1-Benzenesulfonyl-3-phenylsulfanyl-2-((E)-styryl)-1H-indole 
• 147752-78-1 diethyl (1-benzenesulfonyl)indol-2-yl methyl phosphonate 
• 98055-05-1 1-Benzenesulfonyl-3-phenylsulfanyl-2-[(E)-2-(3,4,5-trimethoxy-phenyl)-vinyl]-1H-indole 
• 98055-04-0 1-Benzenesulfonyl-2-((E)-2-benzo[1,3]dioxol-5-yl-vinyl)-3-phenylsulfanyl-1H-indole 
• 391653-17-1 1-Benzenesulfonyl-2-[(E)-2-(4,5-dimethoxy-2-nitro-phenyl)-vinyl]-1H-indole 
• 562107-45-3 2-[(E)-2-(4,5-Dimethoxy-2-nitro-phenyl)-vinyl]-1H-indole 

Relevant academic research and scientific papers

Lewis acid-mediated Michaelis-Arbuzov reaction at room temperature: A facile preparation of arylmethyl/heteroarylmethyl phosphonates

A facile preparation of arylmethyl and heteroarylmethyl phosphonate esters was achieved involving a Lewis acid mediated Michaelis-Arbuzov reaction at room temperature. Interaction of arylmethyl halides/alcohols with triethyl phosphite in the presence of Lewis acid at room temperature afforded phosphonate esters in good yields.