105116-40-3

Upstream product

• 72155-45-4 Boc-L-phenylalaninal 
• 51987-73-6 (S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 

Downstream Products

• 139163-87-4 (2R,3S)-methyl 3-amino-2-hydroxy-4-phenylbutanoate 
• 211677-18-8 (2R,3S)-2-Hydroxy-3-[(1H-indole-2-carbonyl)-amino]-4-phenyl-butyric acid 
• 186392-33-6 (2R,3S)-3-[(5-Fluoro-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid 
• 186392-34-7 (2R,3S)-3-[(5-Bromo-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid 
• 211677-17-7 (2R,3S)-2-Hydroxy-3-[(1H-indole-2-carbonyl)-amino]-4-phenyl-butyric acid methyl ester 
• 186392-11-0 (2R,3S)-3-[(5-Fluoro-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid methyl ester 
• 186392-12-1 (2R,3S)-3-[(5-Bromo-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid methyl ester 
• 186392-32-5 (2R,3S)-3-[(5-Chloro-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid 
• 186392-22-3 (2R,3S)-3-[(5-Chloro-1H-indole-2-carbonyl)-amino]-2-hydroxy-4-phenyl-butyric acid methyl ester 
• 186392-40-5 [R-(R*,S*)]-5-chloro-N-[3-(dimethylamino)-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-1H-indole-2-carboxamide 
• 142489-20-1 tert.-butyl [(1S,2R)-1-benzyl-2-(cyclopropylcarbonyl)-2-hydroxyethyl]carbamate 
• 143238-35-1 C₂₁H₃₈N₂O₃Si 
• 1400634-52-7 [(1S,2S)-1-benzyl-3-benzylamino-2-(tert-butyl(dimethyl)silanyloxy)propyl]carbamic acid tert-butyl ester 
• 1400634-53-8 [(1S,2S)-3-(acetyl(benzyl)amino)-1-benzyl-2-(tert-butyl(dimethyl)silanyloxy)propyl]carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Nonpeptidic lysosomal modulators derived from Z-Phe-Ala-diazomethylketone for treating protein accumulation diseases

Lysosomes are involved in protein turnover and removing misfolded species, and their enzymes have the potential to offset the defect in proteolytic clearance that contributes to the age-related dementia Alzheimer's disease (AD). The weak cathepsin B and L

Unique Stereocontrol in Europium (III)-Catalyzed Cyanosilylation of chiral α-Alkoxy and α-Amino Aldehydes

The Eu(III)-catalyzed cyanosilylations of chiral α-alkoxy and α-amino aldehydes are shown to exhibit syn diastereofacial selection, the degree increasing with an increase in steric bulk of the alkyl chain in the aldehydes.The mechanism of this catalytic p