938069-18-2

Upstream product

• 1225072-47-8 C₁₆H₂₁BrN₂O₂ 
• 67-56-1 methanol 
• 42538-40-9 (S)-2-amino-3-(2-bromophenyl)propanoic acid 

Downstream Products

• 1225072-53-6 C₂₀H₂₇BrN₂O₅ 
• 1225072-49-0 C₂₁H₃₁BrN₂O₅ 
• 1365533-56-7 (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline 
• 1365533-66-9 1-((1R,3S)-3-(((tert-butyldimethylsilyl)oxy)methyl)-2-tosyl-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one 
• 1365533-58-9 1-((1S,3S)-3-(((tert-butyldimethylsilyl)oxy)methyl)-2-tosyl-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one 
• 1365533-59-0 butyl 2-((1S,3S)-3-(((tert-butyldimethylsilyl)oxy)methyl)-2-tosyl-1,2,3,4-tetrahydroisoquinolin-1-yl)acetate 
• 1365533-55-6 (S)-N-(1-(2-bromophenyl)-3-((tert-butyldimethylsilyl)oxy)propan-2-yl)-p-toluenesulfonamide 
• 1365533-54-5 (S)-methyl 3-(2-bromophenyl)-2-(p-toluenylsulfonamido)propanoate 
• 141410-06-2 (S)-indoline-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Specific Inhibitor of Placental Alkaline Phosphatase Isolated from a DNA-Encoded Chemical Library Targets Tumor of the Female Reproductive Tract

Placental alkaline phosphatase (PLAP) is an abundant surface antigen in the malignancies of the female reproductive tract. Nevertheless, the discovery of PLAP-specific small organic ligands for targeting applications has been hindered by ligand cross-reac

Annulated diketopiperazines from dipeptides or schoellkopf reagents via tandem cyclization-intramolecular N-arylation

Figure presented Facile CuI-mediated N-arylation of diketopiperazine using the Fukuyama modification of the Ullmann-Goldberg reaction can be exploited in new approaches to enantiopure polycyclic diketopiperazines from easily assembled dipeptides or functi