63013-10-5

Upstream product

• 56-41-7 L-alanin 
• 122-01-0 4-chloro-benzoyl chloride 

Downstream Products

• 17896-58-1 Bz(Cl)-Ala-Ser-OCH₃ 
• 93709-84-3 4-ClBz-L-Ala-L-PheOMe 
• 17896-59-2 N--Ala-O-(Z-TF)-Ser-OCH3 
• 17896-63-8 N-(p-Chlor-benzoyl)-Ala-Phe 
• 30334-17-9 N-acetyl-4-chlorobenzamide 
• 56-41-7 L-alanin 
• 74-11-3 para-chlorobenzoic acid 
• 93710-10-2 4-ClBz-D-Ala-L-PheOMe 
• 93709-85-4 4-ClBz-L-Ala-L-ValOMe 
• 93710-11-3 4-ClBz-D-Ala-L-ValOMe 
• 93709-83-2 4-ClBz-L-Ala-L-AlaOMe 
• 93710-09-9 4-ClBz-D-Ala-L-AlaOMe 

Relevant academic research and scientific papers

The Oxidative Decarboxylation of N-Aroylglycines to N-(Aacetoxymethyl)benzamides and N-Formylbenzamides with Lead(IV) Acetate

Treatment of N-aroylglycines that do not bear a strong electron-withdrawing substituents with lead(IV) acetate in acetic acid/acetic anhydride mixtures at 60-100 deg C rapidly gives the corresponding N-(acetoxymethyl)benzamides and N-formylbenzamides in m

N-TERMINAL SUBSTITUENT AND SIDE-CHAIN INFLUENCES ON THE CHEMICAL SHIFTS OF PROTONS IN MODEL DIPEPTIDE SYSTEMS

(1)H Chemical shift values of ester methyls in model dipeptide esters have been shown to be sensitive to (a) the nature and configuration of the constituent amino acids and (b) the spatial distance between the N-terminal aryl group and the ester protons.C