125286-03-5

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 555-16-8 4-nitrobenzaldehdye 
• 6552-67-6 (E)-1-(4-methoxyphenyl)-3-(4-nitrophenyl)-2-propen-1-one 
• 108-24-7 acetic anhydride 
• 39212-16-3 (E)-1-(4-methoxyphenyl)-3-(4-nitrophenyl)prop-2-en-1-ol 

Downstream Products

• 125286-05-7 4-hydroxy-6-methyl-3-<3-(4-methoxyphenyl)-1-(4-nitrophenyl)-2-propen-1-yl>-2-pyrone 
• 125286-04-6 4-hydroxy-6-methyl-3-<1-(4-methoxyphenyl)-3-(4-nitrophenyl)-2-propen-1-yl>-2-pyrone 
• 555-16-8 4-nitrobenzaldehdye 
• 123-11-5 4-methoxy-benzaldehyde 
• 125304-64-5 (E)-3,5-dimethyl-4-<1-(4-methoxyphenyl)-3-(4-nitrophenyl)-2-propen-1-yl>pyrazole 
• 125286-08-0 (Z)-3,5-dimethyl-4-<1-(4-methoxyphenyl)-3-(4-nitrophenyl)-2-propen-1-yl>pyrazole 

Relevant academic research and scientific papers

METHODS AND COMPOSITIONS FOR SUBSTITUTED ARYLCYCLOHEPTANE ANALOGS

In one aspect, the disclosure relates to methods for preparation of intermediates useful for the preparation of aryl-cycloheptene scaffolds. In a further aspect, the disclosed methods pertain to the preparation of compounds comprising an aryl-cycloheptene

Electronic effects in the regioselectivity of nucleophilic attacks on cationic 1,3-diaryl-π-allylpalladium complexes

Nucleophilic attacks on π-allylpalladium complexes derived from O2N-Ph-(CH-CH-CH)-Ph-X systems (X = 4-OMe and 4-Cl) occur preferentially at the allylic terminus remote from the electron-withdrawing group (NO2).