1282061-37-3

Upstream product

• 33005-53-7 5-(4-Methoxy-phenyl)-4-oxo-pentanoic acid ethyl ester 
• 1312844-97-5 ethyl 4-(4-methoxybenzyl)pent-4-enoate 
• 856433-01-7 2-[(4-methoxyphenyl)methyl]prop-2-en-1-ol 

Downstream Products

• 1282061-20-4 C₁₉H₂₁NO₂ 
• 1282060-80-3 C₁₉H₁₉NO₂ 
• 1637370-51-4 (R)-5-(iodomethyl)-5-(4-methoxybenzyl)dihydrofuran-2(3H)-one 

Relevant academic research and scientific papers

Cooperative activation with chiral nucleophilic catalysts and n-haloimides: Enantioselective iodolactonization of 4-arylmethyl-4-pentenoic acids

Chiral triaryl phosphates promote the enantioselective iodolactonization of 4-substituted 4-pentenoic acids to give the corresponding iodolactones in high yields with high enantioselectivity. N-Chlorophthalimide (NCP) is employed as a Lewis acidic activat

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.