253328-41-5

Upstream product

• 50-00-0 formaldehyd 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 
• 1826-67-1 vinyl magnesium bromide 
• 253328-37-9 2-(p-methoxyphenyl)ethanol-1,1,2-d3 
• 253328-38-0 2-(p-methoxyphenyl)ethyl 1,1,2-d3 bromide 

Downstream Products

• 1046834-56-3 (E)-methyl (3-(4-methoxyphenyl)allyl)(tosyl)carbamate 
• 1239669-08-9 C₁₉H₂₀⁽²⁾HNO₅S 
• 1350764-19-0 methyl (E)-4-deutero-4-(4-methoxyphenyl)-3-butenoate 
• 24680-50-0 4-methoxy-trans-cinnamaldehyde 
• 1268248-71-0 C₁₀H₉⁽²⁾HO₂ 

Relevant academic research and scientific papers

Scope and mechanism of allylic C-H amination of terminal alkenes by the palladium/PhI(OPiv)2 catalyst system: Insights into the effect of naphthoquinone

Palladium-catalyzed oxidative amination of unactivated alkyl olefins has been developed to produce linear (E)-allylimides with high regioselectivity. This highly efficient transformation of alkenes has been achieved by enhancing the reoxidation of palladi

Ene Reaction of Arylallyl Alkenes with C60. A Mechanistic Approach

(Matrix Presented) The ene reaction of arylallyl alkenes with C60 occurs either by a concerted mechanism or by the reversible formation of a charged or a dipolar intermediate, followed by the C-H(D) breakage in a rate-limiting step.