39274-71-0

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 123-11-5 4-methoxy-benzaldehyde 
• 20432-03-5 (E)-3-(4-methoxyphenyl)-1-(4-nitrophenyl)-2-propen-1-one 

Downstream Products

• 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 
• 125286-07-9 (E) and (Z)-3-acetyl-4-(4-methoxyphenyl)-6-(4-nitrophenyl)-5-hexen-2-one 
• 125286-06-8 3-acetyl-4-(4-methoxyphenyl)-6-(4-nitrophenyl)hexa-2Z,4-dien-2-ol 
• 125286-09-1 3,5-dimethyl-4-<3-(4-aminophenyl)-1-(4-methoxyphenyl)propyl>pyrazole 
• 125286-02-4 3-(4-methoxyphenyl)-1-(4-nitrophenyl)-2-propen-1-ol acetate 
• 6552-62-1 3-(4-methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one 
• 1377574-63-4 (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene 

Relevant academic research and scientific papers

Electrophilic addition of allylic carbocations to 2-cyclopropylidene-2- arylethanols: A strategy to 3-oxabicyclo[3.2.0]heptanes

We have developed an electrophilic addition of allylic carbocations to 2-cyclopropylidene-2-arylethanols constructing carbon-carbon bonds with excellent regio- and stereoselectivities. The reaction affords 3-oxabicyclo[3.2.0]heptanes in moderate to good y

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).