28238-46-2

Upstream product

• 21535-97-7 3-methyl-benzofuran 
• 90-02-8 salicylaldehyde 
• 695-84-1 2-allylphenol 
• 1345020-36-1 1,2-bis(2-hydroxybenzoyl)-1-propanone 
• 10366-02-6 2-Methoxyphenylmercuric chloride 

Downstream Products

• 148120-56-3 2-(2'-tert-butyldimethylsiloxy)phenyl-3-methylbenzofuran 
• 145723-26-8 2a-(2-Acetoxyphenyl)-2a,7b-dihydro-7b-methyl-1,2-dioxeto<3,4-b>benzofuran 
• 53278-17-4 2-(2-Acetoxybenzoyloxy)acetophenone 
• 148120-58-5 2a,7b-dihydro-2a-(2'-tert-butyldimethylsiloxy)phenyl-7b-methyl-1,2-dioxeto<3,4-b>benzofuran 
• 145723-30-4 2-(2-Hydroxybenzoyloxy)acetophenone 
• 28238-47-3 Acetic acid 2-(3-methyl-benzofuran-2-yl)-phenyl ester 

Relevant academic research and scientific papers

Aerobic Copper-Catalyzed Intramolecular Cascade Oxidative Isomerization/[4+4] Cyclization of 2,2′-Disubstituted Stilbenes

An aerobic copper-catalyzed cascade oxidative isomerization/[4+4] cyclization of 2,2′-disubstituted stilbenes is described. Under the mild CuCl/DBED/air catalytic system, various 5,10-heteroatom-containing tetrahydroindeno[2,1-a]indenes were efficiently p

Catalytic hydroacylation as an approach to homoaldol products

A method has been developed for the intermolecular hydroacylation of homoallyl alcohols with salicylaldehydes to furnish homoaldol products in 50-98% yields. The method also applies to the hydroacylation of 2-hydroxystyrenes. This work highlights the use of hydroacylation as a unified approach to both aldol and homoaldol products.

Base-Induced Chemiluminescence of Acetoxy-Substituted Benzofuran Dioxetanes by an Intramolecular Electron Transfer (CIEEL) Mechanism

Tetraphenylporphine-sensitized photooxygenation of acetoxy-substituted benzofuran derivatives 2 afforded the corresponding benzofuran dioxetanes 3.The base-induced decomposition of these dioxetanes was studied and shown to involve an intramolecular CIEEL