1224969-79-2

Upstream product

• 100-52-7 benzaldehyde 
• 120-72-9 indole 
• 1373935-52-4 tert-butyl N-[phenyl(2,4,6-trimethoxyphenyl)methyl]carbamate 
• 1190880-12-6 1,2,4-trimethoxy-5-(phenyl(p-toluenesulfonyl)methyl)benzene 

Relevant academic research and scientific papers

Facile synthesis of nonsymmetrical heteroaryl-substituted triarylmethanes: Via the FeCl3·6H2O-catalyzed two-step Friedel-Crafts-type reaction

The FeCl3·6H2O-catalyzed three-component aza-Friedel-Crafts reaction of aromatic/heteroaromatic compounds, aromatic aldehydes and tert-butyl carbamate was reported. The subsequent Friedel-Crafts-type alkylation of the resulting tert-

Regioselective arylations of α-amido sulfones with electron-rich arenes through friedel-crafts alkylations catalyzed by ferric chloride hexahydrate: Synthesis of unsymmetrical and bis-symmetrical triarylmethanes

Ferric chloride hexahydrate is a highly efficient catalyst for the regioselective arylation of α-amido sulfones. The products undergo further Friedel-Crafts alkylations with heteroaromatic or electron-rich arenes to afford unsymmetrical or bis-symmetrical