15817-51-3

Upstream product

• 95091-92-2 N-methoxy-N-methyl-2-furancarboxamide 
• 352-13-6 4-flourophenylmagnesium bromide 
• 527-69-5 2-furancarbonyl chloride 
• 13331-23-2 fur-2-ylboronic acid 
• 456-22-4 4-Fluorobenzoic acid 
• 437-29-6 tris(4-fluorophenyl)bismuthane 

Downstream Products

• 1263191-86-1 4-fluorophenyl[5-(4-nitrophenyl)furan-2-yl]methanone 
• 1263191-92-9 4-fluorophenyl(5-phenylfuran-2-yl)methanone 
• 1263191-91-8 4-fluorophenyl[5-(4-fluorophenyl)furan-2-yl]methanone 
• 1263191-89-4 1-{4-[5-(4-fluorobenzoyl)furan-2-yl]phenyl}ethanone 
• 1263191-87-2 4-fluorophenyl[5-(4-methoxyphenyl)furan-2-yl]methanone 
• 1263191-85-0 4-[5-(4-fluorobenzoyl)furan-2-yl]benzonitrile 
• 1263191-82-7 methyl 4-[5-(4-fluorobenzoyl)furan-2-yl]-2-hydroxybenzoate 
• 1263191-88-3 ethyl 4-[5-(4-fluorobenzoyl)furan-2-yl]benzoate 
• 1263191-93-0 5-[5-(4-fluorobenzoyl)furan-2-yl]-1,3-dimethylpyrimidine-2,4(1H,3H)-dione 
• 380878-55-7 γ-(p-fluorophenyl)-γ-(2-furyl)propylamine 
• 879218-23-2 (E)-3-(4-Fluoro-phenyl)-3-furan-2-yl-acrylonitrile 
• 111609-56-4 1-(4-Fluoro-phenyl)-3,4-dihydro-pyrrolo[1,2-a]pyrazine 

Relevant academic research and scientific papers

Method Of Preparing Fused Ring Indeno Compounds

The present invention relates to methods of preparing fused ring indeno compounds that involves reacting together a dienophile and a lactone compound, in the presence of a catalyst, and a carboxylic acid anhydride. With some embodiments, the fused ring in

Arylation of 2-furyl 4-fluorophenyl ketone: An extension of heck chemistry towards novel integrase inhibitors

An optimized procedure for the direct and regioselective arylation of 2-acylfurans has been developed. The versatility of this protocol has been evaluated on a series of aryl and heteroaryl halides, thus obtaining a small collection of 2,5-disubstituted f

Atom-efficient cross-coupling reactions of triarylbismuths with acyl chlorides under Pd(0) catalysis

The atom-efficient cross-coupling reaction of triarylbismuths with a variety of aliphatic, aromatic, and hetero-aromatic acyl chlorides was demonstrated to afford high yields of cross-coupled ketones under palladium catalysis. The corresponding cross-coupling reaction with diacid chlorides also furnished bis-coupled ketones in good yields.

A short synthesis of 3,3-di(hetero)arylpropylamines obtained from bis-(hetero)aryl ketones via palladium catalysis

A palladium-catalyzed parallel synthesis of bis-hetero(aryl) ketones is described with two further synthetic steps allowing easy entry to 3,3-di(hetero)arylpropylamines.