54394-61-5

Upstream product

• 673-32-5 1-Phenylprop-1-yne 
• 1576-37-0 N-benzyl-p-toluenesulfonamide 
• 171037-07-3 (S)-(-)-1-phenyl-prop-2-enyl methyl carbonate 
• 87802-71-9 (E)-methyl cinnamyl carbonate 

Downstream Products

• 20442-73-3 (1E)-3-(4-methoxyphenyl)-1-phenylpropene 

Relevant academic research and scientific papers

Highly enantioselective iridium-catalysed allylic aminations with anionic N-nucleophiles

Iridium-catalysed allylic substitutions with anionic N-nucleophiles were achieved with regioselectivity of up to 49:1 and enantiomeric excess of up to 98%. The Royal Society of Chemistry 2005.

Hydroamination of alkynes catalyzed by palladium/benzoic acid

The reaction of internal alkynes (1) with amines (2) in the presence of catalytic amount of Pd(PPh3)4 and benzoic acid in dioxane at 100°C gave the allylic amines (3) in good to excellent yields. The intramolecular reaction of alkyne