1032583-04-2

Upstream product

• 135822-89-8 (E)-N-(benzo[d][1,3]dioxol-5-ylmethylene)-4-methylbenzenesulfonamide 
• 98-80-6 phenylboronic acid 
• 135822-89-8 N-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-4-methyl-benzenesulfonamide 
• 1426578-34-8 C₁₅H₁₄O₃ 
• 70-55-3 toluene-4-sulfonamide 
• 4382-91-6 1,3-benzodioxol-5-yl(phenyl)methanol 

Relevant academic research and scientific papers

Iron-catalyzed N-alkylation using π-activated ethers as electrophiles

A new method for the synthesis of diverse N-alkylation compounds was developed via an iron-catalyzed etheric Csp3-O cleavage with the C-N bond formation in the reaction of π-activated ethers with various nitrogen-based nucleophiles. In addition, the mechanism of this reaction was investigated. The Royal Society of Chemistry 2013.

Palladium(II)/2,2′-bipyridine-catalyzed addition of arylboronic acids to N-tosyl-arylaldimines

A Pd(II)/NO2-bpy-catalyzed addition of the arylboronic acids to N-tosylaldimines to yield diarylmethylamines with moderate to excellent yield was developed. The use of bipyridines as the ligands is crucial in this reaction. The asymmetric versi

Palladium-catalyzed addition of arylboronic acids to N-tosylarylimines

Pd-catalyzed addition of arylboronic acids to N-tosylarylimines was described by employing easily prepared, air-stable aminophosphine ligands, cheap inorganic base, and common organic solvents, providing diarylmethylamine derivatives through one-pot synth