128254-49-9

Upstream product

• 21286-78-2 methyl N-benzoyl-2-methoxyglycinate 
• 20989-42-8 N-benzoylserine methyl ester 
• 101649-82-5 N-benzoyl-2-bromoglycine methyl ester 
• 1205-08-9 methyl hippurate 
• 5673-89-2 N-benzoylcysteine methyl ester 
• 5673-91-6 N,N'-dibenzoylcystine dimethyl diester 
• 110339-43-0 N-benzoyl-α-benzoyloxyglycine methyl ester 

Downstream Products

• 24153-31-9 2-benzoylaminoacrylic acid methyl ester 
• 56538-67-1 N-benzoyl-2-methylthioglycine methyl ester 
• 128254-57-9 dimethyl 2,6-benzamido-4-thiaheptanedioate 

Relevant academic research and scientific papers

Reactions of α-substituted glycine derivatives with stannanes

α-Benzoyloxy- and α-methoxy-substituted glycine derivatives are more stable than the corresponding bromides, yet they undergo analogous reactions with stannanes. Their reactions with mixtures of hexabutylditin and dialkyl disulphides give α-alkylthio-subs

Synthesis of Novel Cross-Linked Amino Acid Derivatives

Reactions of the derivatives of cysteine (6), serine (7) and lysine (8a), with the bromide (1), afforded the corresponding cross-linked amino acid derivatives (11), (12) and (13).Of the linked species (11)-(13), the cysteine derivative (11) was found to be the most stable under a variety of conditions.A mixture of the cross-linked serine derivative (12) and the cysteine derivative (6) in chloroform containing triethylamine reacted to give the cross-linked cysteine derivative (11) and the serine derivative (7).Similarly, a mixture of (13) and (6) in chloroform reacted to give (11).