76075-53-1

Upstream product

• 26086-60-2 2-azido-4'-chloroacetophenone 
• 104-87-0 4-methyl-benzaldehyde 
• 19672-63-0 1-(4-chlorophenyl)-3-(4-methylphenyl)prop-2-en-1-one 

Downstream Products

• 110010-07-6 Z-1-(4-chlorophenyl-)-2-amino-3-(4-tolyl-)-propene-2-one-1 
• 110010-09-8 E-1-(4-chlorophenyl-)-2-acetamido-3-(4-tolyl-)-propene-2-one-1 
• 110010-08-7 Z-1-(4-chlorophenyl-)-2-acetamido-3-(4-tolyl-)-propene-2-one-1 
• 117825-87-3 1-(4-chlorophenyl-)-3-(4-tolyl-)-propane-2-one-1 
• 1361316-73-5 (4-chlorophenyl)[5-(4-methylphenyl)-2-phenyloxazol-4-yl]methanol 
• 344426-62-6 1-(4-chlorophenyl)-3-(p-tolyl)-2-((triphenylphosphoranylidene)amino)prop-2-en-1-one 
• 1427302-20-2 1-(4-(4-chlorobenzoyl)-2-methyl-5-p-tolyl-1H-pyrrol-3-yl)ethanone 
• 1427302-43-9 1-(4-(4-chlorobenzoyl)-2-methyl-5-p-tolyl-1H-pyrrol-3-yl)-2,2,2-trifluoroethanone 
• 110010-13-4 Z-1-(4-chlorophenyl-)-2-(N,N-diacetylamino-)-3-(4-tolyl-)-propene-2-one-1 
• 76075-55-3 1-(p-chlorophenyl-)-2-(triphenylphosphazeno-)-3-(p-tolyl-)-2-propene-1-one 

Relevant academic research and scientific papers

Indium trichloride catalyzed regioselective synthesis of substituted pyrroles in water

A facile and regioselective synthesis of polysubstituted pyrroles from α-azido chalcones and 1,3-dicarbonyl compounds is described. Indium trichloride in water is found to be efficient in catalyzing this transformation.

Unexpected synthesis of 2,4,5-trisubstituted oxazoles via a tandem aza-wittig/michael/isomerization reaction of vinyliminophosphorane

2,4,5-Trisubstituted oxazoles 6 were unexpectedly prepared from a tandem reaction of vinyliminophosphorane 3 with various acyl chlorides in a one-pot fashion.

cis-trans-Configuration of α-Azidochalkones

The two stereoisomeric α-azidochalkones (1,3-diaryl-2-azidopropenones) are selectively obtainable, depending on the temperature, by condensation of aldehydes with α-azidocarbonyl compounds.For the higher melting point compound the trans configuration is p