76553-88-3

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 24680-50-0 4-methoxy-trans-cinnamaldehyde 
• 62-53-3 aniline 

Downstream Products

• 76553-89-4 [(E)-3-(4-Methoxy-phenyl)-prop-2-en-(E)-ylidene]-phenyl-amine; compound with trichloro-acetic acid 
• 1394171-52-8 (E)-N-(4-(4-methoxyphenyl)but-3-en-2-yl)aniline 
• 1394171-65-3 (E)-N-((E)-4-(4-methoxyphenyl)but-3-en-2-ylidene)aniline oxide 
• 1394171-65-3 (Z)-N-((E)-4-(4-methoxyphenyl)but-3-en-2-ylidene)aniline oxide 
• 1739-13-5 N-phenyl-3-(4-methoxyphenyl)propane-1-amine 
• 132931-48-7 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-[(E)-2-(4-methoxy-phenyl)-vinyl]-4-phenyl-4,5-dihydro-[1,2,4]oxadiazole 
• 1372125-77-3 4-(4-methoxyphenyl)-1-phenyl-1,4-dihydroquinoline 
• 1372125-98-8 (E)-2-(4-methoxystyryl)-N-phenyl-1,2-dihydrobenzo[b]azete 
• 1372126-00-5 2-(4-methoxyphenyl)-1-phenyl-1,2-dihydroquinoline 

Relevant academic research and scientific papers

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

Synthesis of aryl-substituted 1,4-dihydroquinolines by [4+2] cycloaddition of benzyne with 1-azadienes

The synthesis of aryl-substituted 1,4-dihydroquinolines can be achieved using a [4+2] cycloaddition between benzyne and various aryl-substituted 1-azadienes. The conditions are tolerated by N-aryl-, alkyl-, tosyl-, and tert-butoxycarbonyl-protected 1-azad

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

Synthesis, Molecular Structure, Fluxional Behavior, and Tricarbonyliron Transfer Reactions of (η4-1-Azabuta-1,3-diene)tricarbonyliron Complexes

The η4-1-azabuta-1,3-diene)tricarbonyliron complexes 10 are easily prepared in high yield by condensation of the corresponding arylamines 7 with the cinnamaldehydes 8 and subsequent ultrasound-promoted complexation of the resulting 1-azabuta-1,3-dienes 9 with nonacarbonyldiiron. The complexes 10 are shown to represent excellent reagents for the transfer of the tricarbonyliron fragment onto cyclohexa-1,3-diene (1a). The structural characterization for the complexes 10 is achieved by IR, 1H-NMR, and 13C-NMR spectroscopy, as well as X-ray crystallography of 10b, 10c, and 101. Using variable temperature 13C-NMR spectroscopy the fluxionality of the complexes 10a, 10b, 10c, 10e, and 2 is investigated and the activation barrier for the turnstile rotation of the tricarbonyliron fragment is determined. The transfer reaction and the structural factors influencing the transfer of the tricarbonyliron fragment are extensively investigated.