103225-18-9

Upstream product

• 90656-99-8 (S)-N-[3-Chloro-2-oxo-1-(phenylmethyl)propyl]-benzamide 
• 103225-23-6 (S)-Alanin-(2-trimethylsilylethyl)ester 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 103225-22-5 (S)-2-[((2R,3S)-2-Acetoxy-3-benzoylamino-4-phenyl-butyl)-benzyloxycarbonyl-amino]-propionic acid 2-trimethylsilanyl-ethyl ester 
• 96922-75-7 (S)-1-[(S)-2-((2R,3S)-3-Benzoylamino-2-hydroxy-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid; hydrochloride 
• 96922-75-7 (S)-1-[(S)-2-((2S,3S)-3-Benzoylamino-2-hydroxy-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid; hydrochloride 
• 103225-20-3 (S)-1-{(S)-2-[((S)-3-Benzoyl-4-benzyl-2,2-dimethyl-oxazolidin-5-ylmethyl)-benzyloxycarbonyl-amino]-propionyl}-pyrrolidine-2-carboxylic acid benzyl ester 
• 103225-19-0 (S)-2-[((S)-3-Benzoyl-4-benzyl-2,2-dimethyl-oxazolidin-5-ylmethyl)-benzyloxycarbonyl-amino]-propionic acid 2-trimethylsilanyl-ethyl ester 

Relevant academic research and scientific papers

Synthesis of Peptide-Derived Amino Alcohols. 1. Potential Transition-State Inhibitors of Angiotensin Converting Enzyme

Synthetic methods and protection schemes were developed for "peptidyl amino alcohols" in which a novel "amino alcohol" design element is introduced into a peptide backbone to produce a new class of proteolytic enzyme inhibitors.