1282060-80-3

Upstream product

• 856433-01-7 2-[(4-methoxyphenyl)methyl]prop-2-en-1-ol 
• 1282061-20-4 C₁₉H₂₁NO₂ 
• 1282061-37-3 4-(4-methoxybenzyl)pent-4-enoic acid 
• 62-53-3 aniline 
• 1312844-97-5 ethyl 4-(4-methoxybenzyl)pent-4-enoate 

Relevant academic research and scientific papers

Pd(II)-catalyzed intramolecular amidoarylation of alkenes with molecular oxygen as sole oxidant

Stereoselective palladium-catalyzed synthesis of structurally versatile indoline derivatives, using molecular oxygen as the sole oxidant, is described. New C-N and C-C bonds form across an alkene in an intramolecular manner. The C-N bond-forming step proceeds via a syn-amidopalladation pathway. The moderate kinetic isotope effects (intramolecular KIE = 3.56) suggest that electrophilic aromatic substitution occurs in the arylation step.