918161-08-7

Upstream product

• 918161-13-4 acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-14-5 (R)-2-hydroxy-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-15-6 acetic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-07-6 rac-acetic acid 1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 

Downstream Products

• 918161-09-8 methanesulfonic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-11-2 toluene-4-sulfonic acid (S)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 918161-13-4 acetic acid (R)-1-(4-methoxy-benzylcarbamoyl)-2-phenyl-ethyl ester 
• 673-06-3 D-(R)-phenylalanine 
• 2448-45-5 Cbz-D-Phe 
• 28069-46-7 D-phenylalanine hydrochloride 
• 918161-12-3 (R)-2-azido-N-(4-methoxybenzyl)-3-phenyl-propionamide 
• 918161-10-1 (R)-2-amino-N-(4-methoxy-benzyl)-3-phenyl-propionamide 

Relevant academic research and scientific papers

Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics

A new, efficient method for the multicomponent synthesis of tripeptide mimetics is presented. Simple, chemoenzymatic transformations of Passerini reaction products enable the introduction of varied amino acid moieties into the tripeptide scaffold, with co

Multicomponent diversity and enzymatic enantioselectivity as a route towards both enantiomers of α-amino acids-a model study

A model study on a new, enantioconvergent method for the synthesis of chiral, nonracemic α-amino acids is presented. α-Acetoxyamides obtained in a Passerini multicomponent reaction are selectively hydrolyzed by Wheat Germ lipase. Studies on conversion of the thus obtained, enantiomerically enriched α-hydroxyamides into α-aminoamides are presented. Products of these reactions are then hydrolyzed to give α-amino acids.