5520-88-7

Upstream product

• 108-94-1 cyclohexanone 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 

Downstream Products

• 82315-14-8 2-Cyclohexyl-4-(4-methoxy-phenyl)-octahydro-chromene 
• 82315-13-7 4-(4-Methoxy-phenyl)-2-phenyl-octahydro-chromene 
• 88674-06-0 7-(4-methoxyphenyl)-5-phenyl-4,7,7a,8,9,10,11,11a-octahydrooxazolo[3,2-j]quinoline 
• 27763-18-4 3-Phenyl-5-(4-methoxyphenyl)-2-thiabicyclo<4.4.0>decane 
• 73669-90-6 4-(4-Methoxyphenyl)-2-phenyl-5,6-tetramethylenethiopyrylium trifluoroacetate 
• 41091-63-8 4-(4-methoxyphenyl)-2-phenyl-5,6,7,8-tetrahydroquinoline 
• 5520-89-8 2-phenyl-4-(4-methoxyphenyl)bicyclo<3.3.1>non-2-en-9-one 

Relevant academic research and scientific papers

Synthesis of a New N-Diaminophosphoryl-N'-[(2S)-2-pyrrolidinylmethyl]thiourea as a Chiral Organocatalyst for the Stereoselective Michael Addition of Cyclohexanone to Nitrostyrenes and Chalcones – Application in Cascade Processes for the Synthesis of Polyc

A highly diastereoselective and enantioselective Michael addition of enolizable ketones such as cyclohexanone and acetophenone to a variety of substituted trans-?-nitrostyrenes and chalcones was catalyzed by a novel chiral and unsymmetrical thiourea as or

Three-step synthesis of 2,4-diaryl-5,6,7,8-tetrahydroquinoline derivatives

(Chemical Equation Presented) Addition of cylohexanone to chalcones, obtained from the appropriate acetophenone and benzaldehyde derivatives, under solvent-free conditions gave 1,5-diketones in good yields. Treatment of 1,5-diketones with ammonium acetate in acetic acid afforded directly 2,4-diaryl-5,6,7,8-tetrahydroquinoline derivatives (7a-u) in high yields. The structures of 7a-u were elucidated by 1H NMR, 13C NMR, IR, and elemental analysis.