104581-50-2

Upstream product

• 66-25-1 hexanal 
• 768-60-5 4-methoxyphenylacetylen 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 104581-58-0 1,1-Bis-(4-methoxy-phenyl)-oct-1-en-3-one 
• 104581-52-4 1,1-Bis-(4-methoxy-phenyl)-oct-1-en-3-ol 
• 104581-55-7 (Z)-1,2-Bis-(4-methoxy-phenyl)-oct-1-en-3-ol 

Relevant academic research and scientific papers

Copper-catalyzed arylative meyer-schuster rearrangement of propargylic alcohols to complex enones using diaryliodonium salts

Free choice: A copper-catalyzed arylative Meyer-Schuster rearrangement is described. The reaction is compatible with a range of substituted propargylic alcohols and diaryliodonium salts and delivers complex trisubstituted enone products selectively as the

Facile one-pot synthesis of functionalized acetylenes from aryl and heteroaryl aldehydes using lithium trimethylsilyldiazomethane

The reaction of aryl and heteroaryl aldehydes with lithium trimethylsilyldiazomethane followed by treatment with n-BuLi and then electrophiles in one-pot efficiently afforded functionalized acetylenes.