14382-03-7

Upstream product

• 1023-17-2 4-methoxyphenyl benzyl ketone 
• 611-94-9 4-Methoxybenzophenone 
• 6921-34-2 benzylmagnesium chloride 
• 451-40-1 phenyl benzyl ketone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 100-44-7 benzyl chloride 

Downstream Products

• 72474-39-6 4-(1,2-diphenylvinyl)anisole 
• 1233-23-4 (E)-1-(4-methoxyphenyl)-1,2-diphenylethylene 
• 1233-23-4 (Z)-1-(4-methoxyphenyl)-1,2-diphenylethylene 
• 131544-74-6 (E)-1,1-dichloro-2,3-diphenyl-2-(4-methoxyphenyl) cyclopropane 
• 131544-74-6 (Z)-1,1-dichloro-2,3-diphenyl-2-(4-methoxyphenyl) cyclopropane 
• 72474-42-1 (Z)-(1-chloro-2-(4-methoxyphenyl)ethene-1,2-diyl)dibenzene 
• 72474-38-5 (E)-(1-chloro-2-(4-methoxyphenyl)ethene-1,2-diyl)dibenzene 

Relevant academic research and scientific papers

Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols

The one-pot conversion of thioenols into benzo[b]thiophenes was achieved by using a simple palladium catalyst such as PdCl2 or PdCl 2(cod). The Royal Society of Chemistry.

Synthesis and chiral separation of some antitumor agents

Four Z-isomers of 1,1-dichloro-2,2,3-triarylcyclopropane (DTACs), designed as potent antitumor agents, were synthesized from their appropriately substituted ethenes, which were prepared from the Grignard reaction followed by the dehydration of their inter

Triarylcyclopropanes as antiestrogens and antitumor agents

Triarylcyclopropane derivatives in which one or more of the aryl groups includes a hydroxy as a substituted or unsubstituted or alkoxy or side chain substituent. The compounds are useful as antiestrogens and anti-tumor agents.