1352007-65-8

Upstream product

• 136207-26-6 (S)-2-((tert-butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid 

Downstream Products

• 479682-15-0 (S)-2-amino-3-(4-azido-2,3,5,6-tetrafluoro-phenyl)-propionic acid 
• 1336536-11-8 C₉H₆BrF₄NO₂ 
• 1336171-10-8 C₉H₆ClF₄NO₂ 
• 1352007-70-5 (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-bromo-2,3,5,6-tetrafluorophenyl)propanoic acid 
• 1352007-69-2 (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-chloro-2,3,5,6-tetrafluorophenyl)propanoic acid 
• 1352007-68-1 (S)-3-(4-amino-2,3,5,6-tetrafluorophenyl)-2-(2,2,2-trifluoroacetamido)propanoic acid 
• 1352007-67-0 (S)-3-(4-azido-2,3,5,6-tetrafluorophenyl)-2-(2,2,2-trifluoroacetamido)propanoic acid 
• 1352007-66-9 (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-amino-2,3,5,6-tetrafluorophenyl)propanoic acid 

Relevant academic research and scientific papers

A halogen bond-donor amino acid for organocatalysis in water

Herein we report a halogen bond-donor amino acid, 4-iodotetrafluorophenylalanine, which behaves as a catalyst for the aqueous synthesis of bis-(heterocyclic)methanes. We also provide experimental evidence that halogen bonding is a plausible explanation fo

Synthesis of tetrafluorinated aromatic amino acids with distinct signatures in 19F NMR

Fluorinated amino acids serve as powerful tools in protein chemistry. We synthesized a series of para-substituted tetrafluorophenylalanines via the regioselective SNAr chemistry of the commercially available pentafluorophenylalanine Boc-Z. Thes