85636-82-4

Upstream product

• 69511-77-9 1-(4,5-dimethoxy-2-nitrophenyl)-2-phenyl-1-ethanone 
• 103-82-2 phenylacetic acid 
• 69511-74-6 3-(4,5-Dimethoxy-2-nitro-phenyl)-3-oxo-2-phenyl-propionaldehyde 
• 103-80-0 phenylacetyl chloride 
• 3141-93-3 4',5'-dimethoxydeoxybenzoin 
• 91-16-7 1,2-dimethoxybenzene 

Downstream Products

• 37514-62-8 4-benzyl-6,7-dimethoxyquinazoline 
• 924635-52-9 4,5-dimethoxy-2-[1-(5-methyl-2-furyl)-2-phenylethyl]-1-(4-methylphenylsulfonamido)benzene 
• 924635-47-2 2-(1-hydroxy-2-phenylethyl)-4,5-dimethoxy-1-(4-methylphenylsulfonamido)benzene 
• 886493-72-7 4,5-dimethoxy-1-(4-methylphenylsulfonamido)-2-(2-phenylacetyl)benzene 

Relevant academic research and scientific papers

Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction

A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.

o-Aminophenyl Alkyl/Aralkyl Ketones and Their Derivatives: Part IV - Synthesis of 4-Benzyl-6,7-dimethoxyquinazoline

o-Nitrophenyl benzyl ketones (II) have been exclusively synthesised from the corresponding substituted α-(o-nitroaroyl)arylacetaldehydes by the acid-catalysed deformylation.Nitration of deoxybenzoins having one of the benzene nuclei activated, such as the