66383-09-3

Upstream product

• 1142-20-7 N-Cbz-Ala 
• 55446-83-8 Proline Ethylamide 
• 557-66-4 ethanamine hydrochloride 
• 21027-01-0 N-benzyloxycarbonyl-L-alanyl-L-proline 
• 55446-83-8 N-ethyl-prolinamide 
• 543-27-1 isobutyl chloroformate 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
• 55446-81-6 Benzyloxycarbonylproline Ethylamide 

Downstream Products

• 84899-53-6 Alanyl-proline Ethylamide 
• 84914-63-6 Benzyloxycarbonylalanyl-alanyl-proline Ethylamide 
• 83808-37-1 4-{(S)-1-[(S)-2-((S)-2-Ethylcarbamoyl-pyrrolidin-1-yl)-1-methyl-2-oxo-ethylcarbamoyl]-ethylcarbamoyl}-butyric acid 

Relevant academic research and scientific papers

Activation of carboxylic acids by pyrocarbonates: Synthesis of alkylamides of N-protected amino acids

Alkylamides of amino acids were prepared with high yields via activation of N-protected amino acids by di-tert-butyl pyrocarbonate-pyridine reagent in the presence of alkylamine hydrochlorides and potassium hydrocarbonate.

INHIBITORS OF PANCREATIC AND LEUKOCYTE ELASTASE

Tho following alkylamides of ω-carboxyalkanoyldi- and tripeptides of the Ala-Pro or Ala-Ala-Pro sequence have been prepared: ethylamide-, propylamide-, and isobutylamide of 3-carboxypropionylalanyl-proline, ethylamide of 3-carboxypropionylalanyl-alanyl-pr

Alkylamides of carboxyalkanoyl peptides and method for preparation thereof

A method is described for the preparation of novel alkylamides of carboxyalkanoyl peptides of the formula STR1 wherein R is an aralky or an alkyl group of 1-5 carbon atoms, A is a residue of peptidically bound proline or alanine, B is a straight bond or a