56110-08-8

Upstream product

• 106-47-8 4-chloro-aniline 
• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 132931-54-5 4-(4-Chloro-phenyl)-3-(3,5-dichloro-2,4,6-trimethyl-phenyl)-5-((E)-styryl)-4,5-dihydro-[1,2,4]oxadiazole 
• 37875-83-5 1-(4-chlorophenyl)-2-methyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid ethyl ester 
• 84254-70-6 (1S,6R)-2-Oxo-6-phenyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 116194-97-9 (1S,6R)-3-Methyl-2-oxo-6-phenyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 116194-96-8 (1R,6S)-3-Ethyl-2-oxo-6-phenyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 612-57-7 6-chloroquinoline 
• 1421518-04-8 N-(4-chlorophenyl)-N-[(2E)-3-phenylprop-2-en-1-yl]urea 
• 1394171-48-2 (E)-4-chloro-N-(4-phenylbut-3-en-2-yl)aniline 
• 1394171-60-8 (E)-4-chloro-N-((E)-4-phenylbut-3-en-2-ylidene)aniline oxide 
• 1394171-60-8 (Z)-4-chloro-N-((E)-4-phenylbut-3-en-2-ylidene)aniline oxide 

Relevant academic research and scientific papers

Solvent-free synthesis, DNA-topoisomerase II activity and molecular docking study of new asymmetrically N,N′-substituted ureas

A new series of asymmetrically N,N′-substituted ureas 20-25 was prepared using solvent free conditions, which is an eco-friendly methodology, starting with Schiff bases derived from cinnamaldehyde and p-substituted anilines, which are subsequently submitt

Superacid-promoted synthesis of quinoline derivatives

A series of vinylogous imines have been prepared from anilines and cinnamaldehydes. These substrates react in superacidic media to provide quinolines and related compounds. A mechanism for the conversion is proposed which involves the cyclization of dicationic superelectrophilic intermediates. Aromatization of the quinoline ring is thought to occur by superacid-promoted elimination of benzene.

Insertion of Nitriles into Zirconocene 1-aza-1,3-diene Complexes: Chemoselective Synthesis of N-H and N-Substituted Pyrroles

The direct insertion of nitriles into zirconocene-1-aza-1,3-diene complexes provides an efficient, chemoselective, and controllable synthesis of N-H and N-substituted pyrroles upon acidic aqueous work-up. The outcome of the reaction (that is, the formatio

A modular approach to α,β-unsaturated N-aryl ketonitrones

A modular approach to α,β-unsaturated N-aryl ketonitrones has been developed. Specifically, condensation of anilines and enals followed by alkylation of the resulting α,β-unsaturated imines provided N-allyl anilines, which were subjected to oxidation with

Synthetic and mechanistic studies of indium-mediated allylation of imines in ionic liquids

(Chemical Equation Presented) Aldimines derived from aryl and non-enolizable aliphatic aldehydes were allylated with allyl bromide mediated by indium powder in [bpy][BF4] (bpy = N-butylpyridine) to give good yields of the corresponding homoallylic amines. Selective formation of monoallylated amines can be achieved by varying the amount of bromide ion additive in the form of [bpy][Br]. The transient organoindium intermediates, allylindium-(I) and allylindium(III) dibromide formed in the reaction, were studied by NMR spectroscopy to explain the selectivity.