75350-57-1

Upstream product

• 52071-65-5 N-tert-butyloxycarbonyl-L-prolyl-L-phenylalanine 
• 57177-79-4 (S)-tert-butyl 2-(((S)-1-methoxy-1-oxo-3-phenylpropan-2-yl)carbamoyl)pyrrolidine-1-carboxylate 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 147-85-3 L-proline 

Downstream Products

• 120609-54-3 N^α-Z-L-Arg-L-Arg-L-Pro-L-Phe-L-His-OH 
• 93287-51-5 (S)-2-[(S)-2-({(S)-1-[(S)-2-((S)-2-Benzyloxycarbonylamino-5-guanidino-pentanoylamino)-5-guanidino-pentanoyl]-pyrrolidine-2-carbonyl}-amino)-3-phenyl-propionylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester 
• 93287-31-1 Boc-Pro-His-Pro-Phe-His-OH 
• 120609-81-6 (S)-2-((S)-2-{[(S)-1-((S)-2-Amino-5-guanidino-pentanoyl)-pyrrolidine-2-carbonyl]-amino}-3-phenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester 
• 93287-30-0 (S)-2-[(S)-2-((S)-2-{(S)-1-[(S)-2-(1H-Imidazol-4-yl)-1-methoxycarbonyl-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-pyrrolidin-1-yl)-1-(1H-imidazol-4-ylmethyl)-2-oxo-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Pro-phe derivatives as organocatalysts in asymmetric aldol reaction

The aldol reaction which is the most important one among the C-C bond forming reactions, is widely used by synthetic organic chemists to obtain β-hydroxycarbonyl compounds which are important starting components for biologically active compounds in optica

Renin inhibitors. Synthesis of transition-state analogue inhibitors containing phosphorus cid derivatives at the scissile bond

The synthesis of five amino phosphorus derivatives, 1a-e, is described. The derivatives were incorporated into a series (18) of analogues of the 5-14 portion of angiotensinogen, in most cases at the scissile Leu-Val bond. The resultant compounds were test