128540-54-5

Upstream product

• 128540-53-4 (S)-3-cyclohexyl-2-(isopropoxycarbonyl)aminopropanol 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 124947-31-5 N-(isopropoxycarbonyl)-L-phenylalanine methyl ester 
• 124995-02-4 (S)-N-(isopropoxycarbonyl)phenylalaninol 
• 63-91-2 L-phenylalanine 

Downstream Products

• 128625-50-3 methyl (3R,4S)-5-cyclohexyl-3-hydroxy-4-(isopropoxycarbonyl)aminopentanoate 
• 128625-48-9 methyl (3S,4S)-5-cyclohexyl-3-hydroxy-4-(isopropoxycarbonyl)aminopentanoate 
• 128540-55-6 2-acetoxy-4-cyclohexyl-3-(isopropoxycarbonylamino) butyronitrile 
• 105192-90-3 ACHPA 
• 138448-74-5 methyl <(4S,5R)-4-cyclohexylmethyl-2,2-dimethyl-3-isopropoxycarbonyl-1,3-oxazolidin-5-yl>acetate 
• 138448-73-4 methyl <(4S,5S)-4-cyclohexylmethyl-2,2-dimethyl-3-isopropoxycarbonyl-1,3-oxazolidin-5-yl>acetate 
• 128540-55-6 Acetic acid (R)-1-cyano-3-cyclohexyl-2-isopropoxycarbonylamino-propyl ester 

Relevant academic research and scientific papers

A Practical Synthesis of threo-3-Amino-2-hydroxycarboxylic Acids

An expeditious synthesis of (2R,3S)-3-amino-4-cyclohexyl-2-hydroxybutyric acid (2) and (2S,3R)-3-amino-2-hydroxy-4-phenylbutyric acid (4), the key components of the renin inhibitor (1) and bestatin (3), respectively, have been accomplished by featuring hi

A highly stereoselective synthesis of (3S,4S)-statine and (3S,4S)-cyclohexylstatine

The title compounds, which are synthetic intermediates of renin inhibitors, could be prepared from (S)-leucine and (S)-phenylalanine, respectively, by employing highly stereoselective aldol reactions of O-methyl-O-trimethylsilyl ketene acetal with an (S)-

An expeditious synthesis of (3S,4S)-statine and (3S,4S)cyclohexylstatine

The title synthesis could be accomplished by employing highly stereoselective aldol reaction of O-methyl-O-trimethylsilyl ketene acetal with the (S)-α-amido aldehyde (2) in the presence of titanium (IV) chloride as a key step.