62698-35-5

Upstream product

• 611-94-9 4-Methoxybenzophenone 
• 4440-01-1 lithium phenylacetylide 
• 720-44-5 1-(4-methoxyphenyl)-1-phenylmethanol 
• 536-74-3 phenylacetylene 

Downstream Products

• 1263145-91-0 3-(4-methoxyphenyl)-9-methyl-1,3-diphenyl-3H-pyrrolo[1,2-a]indole 
• 1350930-03-8 2-[3-(4-methoxyphenyl)-1,3-diphenylpropa-1,2-dienyl]-5-methylfuran 
• 1616101-41-7 1-(4-methoxyphenyl)-2,4-diphenyl-9H-carbazole 
• 115037-31-5 3-(4-methoxyphenyl)-4,5-diphenyl-1H-pyrazole 
• 99142-95-7 E/Z-3-(p-methoxyphenyl)-1,3-diphenylprop-2-en-1-one 

Relevant academic research and scientific papers

Tertiary acetylenic alcohols and diols on the basis of phenylacetylene and 2-methyl-3-butyn-2-ol

A procedure has been proposed for the synthesis of tertiary acetylenic alcohols and diols by treatment of phenylacetylene or 2-methyl-3-butyn-2-ol with butyllithium and subsequent reaction of lithium phenylacetylide or lithium 4-lithio-2-methyl-3-butyn-2-

Lewis Acid Catalyzed Cyclization of Propargylic Alcohols with 2-Vinylphenol

An unprecedented Lewis acid catalyzed, protection-free, and high-efficiency synthesis of valuable 3,4-dihydro-2H-2,4-methanochromans via cycloaddition of propargylic alkynols with 2-vinylphenol is described. This cycloaddition protocol, which tolerates a