1005328-49-3

Upstream product

• 117-99-7 2-Hydroxybenzophenone 
• 74-86-2 acetylene 

Downstream Products

• 60312-26-7 (3-phenylbenzofuran-2-yl)acetic acid methyl ester 
• 1005328-59-5 (2-oxo-4-phenyl-2H-chromen-3-yl)acetic acid methyl ester 
• 1609487-30-0 N-tert-butyl-2-(3-phenylbenzofuran-2-yl)acetamide 
• 1609487-45-7 N-cyclohexyl-2-(3-phenylbenzofuran-2-yl)acetamide 
• 1609487-39-9 N-isopropyl-2-(3-phenyllbenzofuran-2-yl)acetamide 
• 856771-93-2 (3-phenyl-1-benzofuran-2-yl)methanol 
• 1060729-16-9 2-methoxymethyl-3-phenyl-1-benzofuran 
• 1060728-90-6 2-methylene-3-phenyl-2,3-dihydro-1-benzofuran-3-ol 
• 57329-33-6 3-phenyl-1-benzofuran-2-carbaldehyde 

Relevant academic research and scientific papers

Copper-Catalyzed Dehydrative Cyclization of 1-(2-Hydroxyphenyl)propargyl Alcohols with P(O)H Compounds for the Synthesis of 2-Phosphorylmethylbenzofurans

A tetrakis(acetonitrile)copper(I) hexafluorophosphate [Cu(MeCN)PF6]-catalyzed dehydrative reaction of 1-(2-hydroxyphenyl)propargyl alcohols with diarylphosphine oxides has been developed to provide an efficient synthesis of phosphorylated benzo

A new copper(I)-catalyzed cycloetherification/acid-catalyzed allylic nucleophilic substitution for one-pot synthesis of 2-substituted benzofurans

A new copper(I)-catalyzed cycloetherification followed by an acid-catalyzed allylic nucleophilic substitution have been developed for the one-pot synthesis of 2-substituted benzofurans. This one-pot reaction proceeds efficiently under extremely mild conditions with simple and inexpensive catalysts, providing diversely substituted benzofurans in good to excellent yields. Georg Thieme Verlag Stuttgart. New York.

A novel palladium-catalyzed dicarbonylation process leading to coumarins

(Chemical Equation Presented) A novel approach to coumarin derivatives has been developed starting from readily available 2-(1-hydroxyprop-2-ynyl)phenols, based on an unprecedented palladium-catalyzed dicarbonylation process. Reactions were carried out in