376594-71-7

Upstream product

• 376594-70-6 N-(R-2-(4-nitrophenyl)-1-propyl)phthalimide 
• 19910-33-9 2-(4-nitrophenyl)propanoic acid 
• 104-03-0 4-nitrobenzeneacetic acid 
• 869304-72-3 4R-benzyl-3-(4-nitrophenylacetyl)-2-oxazolidinone 
• 869304-73-4 4R-benzyl-3-(2R-(4-nitrophenyl)propionyl)-2-oxazolidinone 
• 185130-37-4 R-2-(4-nitrophenyl)-1-propanol 
• 78507-53-6 4-nitrophenylacetyl fluoride 
• 869304-77-8 R-2-(4-nitropheny)-1-propyl azide 

Downstream Products

• 376594-72-8 R-2-(4-nitrophenyl)-1-(2-propanesulfonamido)-propane 
• 376594-64-8 R-2-(4-aminophenyl)-1-(2-propanesulfonamido)-propane 
• 376594-67-1 LY 450108 

Relevant academic research and scientific papers

Synthesis of 14C-labeled and tritiated AMPA potentiator LY450108

Asymmetric synthesis of AMPA potentiator LY450108-[14C] containing 14C-label attached to the chiral center of the molecule, was accomplished based on Evans' chiral oxazolidinone auxiliary method. Diastereoselective methylation of p-n