899452-05-2

Upstream product

• 25726-04-9 phenylglyoxylyl chloride 
• 90-15-3 α-naphthol 
• 611-73-4 Benzoylformic acid 
• 1574666-58-2 2-(naphthalen-1-yloxy)-1-phenyl-2-(2,2,6,6-tetramethylpiperidin-1-yloxy)ethanone 

Downstream Products

• 1361325-96-3 C₂₅H₂₀O₃ 
• 1354509-91-3 (S)-2-hydroxy-1,2-diphenyl-2-(4-methylphenyl)ethanone 

Relevant academic research and scientific papers

Study of enantioselective hydrogenation of bulky esters of phenylglyoxylic acid on Pt-CD and Pt-β-ICN chiral catalysts: Steric effect of ester groups and inversion of enantioselectivity

Enantioselective hydrogenation of seven different esters of phenylglyoxylic acid was investigated by variation of the bulkiness at ester side of the substrates [Ph{single bond}C(O){single bond}C(O)OR, R = Me (l), cyclohexyl (2), adamantyl (3), cis-decahyd

Copper-catalyzed α-aminoxylation of ketones with 2,2,6,6- tetramethylpiperidine-1-oxyl (TEMPO)

An efficient copper-catalyzed α-aminoxylation of ketones with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) is presented for the synthesis of 2-aryloxy-1-aryl-2-(2,2,6,6-tetramethylpiperidin-1-yloxy)ethanones in moderate to excellent yields. It is notewort