1603164-07-3

Upstream product

• 112631-06-8 2-bromo-1-ethenyl-3,4-dihydronaphthalene 
• 1603164-06-2 C₁₂H₁₃BrO 
• 768-60-5 4-methoxyphenylacetylen 
• 112631-07-9 2-bromo-3,4-dihydro-1-naphthaldehyde 

Downstream Products

• 1603163-73-0 C₂₃H₂₂O₂ 
• 1603163-98-9 2-(2-((4-methoxyphenyl)ethynyl)-3,4-dihydronaphthalen-1-yl)-acetaldehyde 
• 1603163-82-1 1-(2-((4-methoxyphenyl)ethynyl)-3,4-dihydronaphthalen-1-yl)-but-3-en-2-ol 
• 1603163-92-3 1-(2-((4-methoxyphenyl)ethynyl)-3,4-dihydronaphthalen-1-yl)-but-3-en-2-one 
• 1603163-59-2 1-(1-(4-methoxyphenyl)vinyl)-9,10-dihydrophenanthrene 
• 1603163-66-1 1-(1-(4-methoxyphenyl)vinyl)-9,10-dihydrophenanthren-3-ol 

Relevant academic research and scientific papers

Synthesis of substituted styrenes and 3-vinylphenols using ruthenium-catalyzed ring-closing enyne metathesis

The synthesis of substituted styrenes 3 and 3-vinylphenols 9 was achieved by ring-closing enyne metathesis (RCEM)/dehydration of 7 and RCEM/tautomerization of 8, respectively. Those methods provide selective access to unique aromatic compounds and solve the problem of regioisomer formation.