1333080-40-2

Upstream product

• 589-29-7 p-xylylene glycol 
• 1333080-48-0 4-((4-methoxybenzyloxy)methyl)benzaldehyde 
• 1333080-39-9 (S)-2-(4-(4-methoxybenzyloxy)phenyl)propan-1-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 1333080-31-1 (4-((4-methoxybenzyloxy)methyl)phenyl)methanol 
• 1333080-37-7 C₂₀H₂₄O₄ 
• 1333080-35-5 2-(4-((4-methoxybenzyloxy)methyl)phenyl)propan-1-ol 
• 1333080-33-3 1-(4-methoxybenzyloxymethyl)-4-isopropenylbenzene 
• 1044064-76-7 1-[4-((4-methoxybenzyloxy)methyl)phenyl]ethanone 

Downstream Products

• 1333080-41-3 {4-[(S)-2-(tert-butyldiphenylsilanyloxy)-1-methylethyl]phenyl}methanol 
• 1333080-42-4 [(S)-2-(4-bromomethylphenyl)propoxy]-tert-butyldiphenylsilane 
• 1333080-43-5 C₃₁H₃₈O₂Si 
• 1333080-44-6 C₃₂H₄₀O₂Si 
• 1333080-45-7 (R)-2-[4-((S)-2-hydroxy-1-methylethyl)benzyl]cyclopentanone 
• 1333080-46-8 (R)-2-[4-((S)-2-hydroxy-1-methylethyl)benzyl]cyclohexanone 
• 1333080-47-9 C₁₆H₂₀O₃ 
• 149056-85-9 (S)-2-[4-((1R)-2-hydroxycyclohexylmethyl)phenyl]propionic acid 
• 149056-83-7 (S)-2-[4-((1R,2S)-2-hydroxycyclohexylmethyl)phenyl]propionic acid 
• 90319-80-5 (2S)-2-<4-(cis-(1R,2R)-2-hydroxycyclopentylmethyl)phenyl>propionic acid 
• 83648-76-4 (2S)-2-<4-(trans-(1R,2S)-2-hydroxycyclopentylmethyl)phenyl>propionic acid 
• 83599-42-2 (2S)-2-<4-((1R)-2-oxocyclopentylmethyl)phenyl>propionic acid 

Relevant academic research and scientific papers

Asymmetric synthesis of the active form of loxoprofen and its analogue

The asymmetric synthesis of the active form of the antiinflammatory drug loxoprofen has been reported in this article. Enzymatic kinetic resolution/racemization of a substituted homo-benzylic primary alcohol with lipase-PS, asymmetric alkylation of cyclic ketones using either Enders' or Meyers' strategy followed by a stereoselective biocatalytic reduction of carbonyl group are the key reactions employed successfully to achieve the target molecule and one of its analogue.