38425-35-3

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 20498-63-9 1-(4-methylphenyl)-2-phenylethanol 
• 716-43-8 dimethyl homophthalate 
• 20511-20-0 ethyl p-methylcinnamate 
• 2001-28-7 2-phenyl-1-p-tolyl-ethanone 
• 14111-33-2 diethyl 2-(4-methylbenzylidene)malonate 
• 60313-51-1 3-p-methylphenyl-2-carboxy-4-phenylbutyric acid 
• 38425-34-2 3-p-methylphenyl-4-phenylbutyric acid 

Downstream Products

• 38425-38-6 1-Methyl-3-(p-tolyl)-tetralin 
• 121511-11-3 3-p-tolylnaphthalen-1-amine 
• 121511-07-7 3-p-Tolyl-3,4-dihydro-2H-naphthalen-1-one oxime 

Relevant academic research and scientific papers

Origin of stereocontrol in guanidine-bisurea bifunctional organocatalyst that promotes α-hydroxylation of tetralone-derived β-ketoesters: Asymmetric synthesis of β- And γ-substituted tetralone derivatives via organocatalytic oxidative kinetic resolution

The mechanism of asymmetric α-hydroxylation of tetralone-derived β-ketoesters with guanidine-bisurea bifunctional organocatalyst in the presence of cumene hydroperoxide (CHP) was examined by means of DFT calculations to understand the origin of the stereo

Synthesis of 3-Aryl-1-tetralones

A new method for the synthesis of 3-aryl-1-tetralones is presented.The tetralones synthesised have been characterised by elemental analysis and soectral data.