1379481-73-8

Upstream product

• 52107-92-3 2-iodo-6-methylbenzoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 54811-50-6 2-iodo-6-methylbenzoic acid 

Downstream Products

• 1379481-58-9 2-((4-fluorophenyl)ethynyl)-N-(4-methoxyphenyl)-6-methylbenzamide 
• 1379481-71-6 C₄₆H₃₄F₂N₂O₄ 
• 1381766-57-9 2-((2-(dimethylamino)-3-methoxyphenyl)ethynyl)-N-(4-methoxyphenyl)-6-methylbenzamide 
• 1381766-42-2 C₂₅H₂₂N₂O₃ 
• 1381766-55-7 2-((2-(dimethylamino)phenyl)ethynyl)-N-(4-methoxyphenyl)-6-methylbenzamide 
• 1381766-41-1 C₂₄H₂₀N₂O₂ 

Relevant academic research and scientific papers

Palladium(II)-catalyzed intramolecular diamination of alkynes under aerobic oxidative conditions: Catalytic turnover of an iodide ion

"I" did it: A sequential intramolecular amination/N- demethylation/amidation of internal acetylenes in the presence of a catalytic amount of Pd(OAc)2 and nBu4NI afforded indolo[3,2-c]isoquinolinones under mild aerobic conditions (see

Synergistic effect of palladium and copper catalysts: Catalytic cyclizative dimerization of ortho-(1-alkynyl)benzamides leading to axially chiral 1,3-butadienes

Two is better than one: In the presence of Pd(OAc)2 and Cu(OAc)2, o-(1-alkynyl)benzamides 1 were converted into bis-iminobenzoisofurans with an axially chiral 1,3-diene 2 unit. The coexistence of both Pd and Cu catalysts was found to be essential for both the cyclizative dimerization process and for the observed unusual cyclization mode. Copyright