22774-84-1

Upstream product

• 106-47-8 4-chloro-aniline 
• 563-47-3 3-Chloro-2-methylpropene 
• 1458-98-6 2-methyl-3-bromo-1-propene 

Downstream Products

• 1202021-60-0 C₁₈H₂₃BrClN 
• 1202021-57-5 C₁₇H₂₁BrClN 
• 1381888-73-8 p-chloro-N-(2-methylallyl)-N-methylaniline 
• 1381888-74-9 3-((4-chlorophenyl)(methyl)amino)-2-methylpropane-1,2-diol 
• 1381888-47-6 4-chloro-N-methyl-N-((2-ethyloxirane-2-yl)methyl)aniline 
• 139944-65-3 1-(4-Chloro-phenyl)-3-methyl-pyrrolidine 
• 55245-24-4 C₁₁H₁₁Cl₂NO 

Relevant academic research and scientific papers

Catalytic, atom-economical radical arylation of epoxides

A slow electron waltz: Catalysis in single-electron steps with radicals as intermediates is essential for an atom-economical arylation of epoxides with a proton-coupled electron transfer as a key step. Stabilization of the catalyst is essential for low catalyst loading, as demonstrated by reaction-progress kinetic analysis, cyclic voltammetry, and calculations. Copyright

Palladium-catalyzed cyclization/cyclopropanation reaction for the synthesis of fused N-containing heterocycles

Palladium-catalyzed cyclization/cyclopropanation can be used to convert a range of substituted cyclic N-aryl allyl/methallyl amines efficiently and selectively to the corresponding fused tetrahydropyridine/cyclopropane-fused isoquinoline derivatives via β