59893-98-0

Upstream product

• 616-34-2 methoxycarbonylmethylamine 
• 121-90-4 m-nitrobenzoic acid chloride 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 121-92-6 3-nitrobenzoic acid 

Downstream Products

• 125700-16-5 α-methoxy-N-(3-nitrobenzoyl)glycine methyl ester 
• 125700-17-6 Dimethoxy-(3-nitro-benzoylamino)-acetic acid methyl ester 
• 56445-69-3 (3-amino-benzoylamino)-acetic acid methyl ester 
• 1027261-92-2 (3-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-benzoylamino)-acetic acid methyl ester 

Relevant academic research and scientific papers

Gastrin and cholecystokinin receptor ligands

Compounds of formula (I) and their pharmaceutically acceptable salts are ligands at gastrin and/or cholecystokinin receptors. X and Y are independently ═N—, —N(R5)—═CH—, —S— or —O—. n is from 1 to 4; R1is H or C1to C1

INDIRECT ELECTROCHEMICAL α-METHOXYLATION OF N-ACYL AND N-CARBOALKOXY α-AMINO ACID ESTERS AND APPLICATION AS CATIONIC GLYCINE EQUIVALENTS

Indirect electrochemical methoxylation of N-acyl and N-carboalkoxy α-amino acid esters in α-position to nitrogen is possible, if chloride is used as mediator.The course of the reaction depends upon the protecting group as well as upon the amino acid side-chain.Increased electron withdrawing effects of the protecting group are accelerating the reaction.On the other hand aliphatic side-chains are diminishing the reactivity.High chloride ion concentrations improve the current yields surprisingly strong.