71897-86-4

Upstream product

• 4333-75-9 1-(4-methoxyphenyl)-1-phenylethene 

Downstream Products

• 68388-12-5 1-(2,2-dibromo-1-phenylvinyl)-4-methoxybenzene 
• 611-94-9 4-Methoxybenzophenone 
• 4333-75-9 1-(4-methoxyphenyl)-1-phenylethene 

Relevant academic research and scientific papers

Acid catalysis in the aminium hexachloroantimonate-induced cyclodimerization of 1-aryl-1-phenylethylenes

The aminium hexachloroantimonate-induced cyclodimerization of various 1-aryl-1-phenylethylenes, affording regioisomeric indane derivatives via a carbocation mechanism, was found to occur in a similar manner when SbCl5 was used instead of the am

Aminium salts-induced dimerization of α-methylstyrene and 1-aryl-1-phenylethylenes. Solvent effect

The aminium salts-induced dimerization of α-methylstyrene 1b gives rise depending on the solvent employed to high yields of 1,3,3-trimethyl-1,3,3-trimethyl-1-phenylindane 2b, or 2,4-diphenyl-4-methyl-1-pentene 6b. Several 1-aryl-1-phenylethylenes 1a,c-e afford, instead, cyclodimers 2a,c-e, or 2,5-diaryl-2,5-diphenyltetrahydrofuran derivatives 3a,c-e.