72374-69-7

Upstream product

• 938-16-9 2,2-dimethylpropiophenone 
• 62-53-3 aniline 
• 582-62-7 3-methyl-1-phenylbutan-1-one 

Downstream Products

• 72374-77-7 N-1-(2,2-Dichlor-3-methyl-1-phenyl-butyliden)-anilin 
• 5650-07-7 3-methyl-1-phenyl-but-2-en-1-one 
• 62269-40-3 2-Chlor-3-methyl-1-oxo-1-phenyl-2-buten 
• 56985-25-2 2-methoxy-3-methyl-1-phenyl-2-buten-1-one 

Relevant academic research and scientific papers

Development of highly enantioselective new Lewis basic N-formamide organocatalysts for hydrosilylation of imines with an unprecedented substrate profile

l-Pipecolinic acid derived N-formamides have been developed as new Lewis basic organocatalysts that promote the asymmetric reduction of N-aryl ketimines using trichlorosilane as the reducing agent. The substituent on N4 of the piperazinyl backbone and the

S-chiral sulfinamides as highly enantioselective organocatalysts

(Diagram presented) Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantioselective organocatalyst relying solely on a chiral sulfur center for stereochemical induction. In the presence of 20 mol % of 2, a broa