620179-39-7

Upstream product

• 2577-48-2 methyl (2S)-pyrrolidine carboxylate 
• 4870-65-9 2-bromophenylacetic acid 
• 226388-27-8 (R)-α-(N,N-dibenzylamino)-α-phenylacetic acid 

Relevant academic research and scientific papers

Stereoselective syntheses of tri- and tetrapeptide analogues by dynamic resolution of α-halo amides in nucleophilic substitution

Dynamic resolution of α-bromo and α-chloro acetamides in nucleophilic substitution with amine nucleophiles in the presence of TBAI has been investigated for stereoselective syntheses of tri- and tetrapeptide analogues. Mechanistic investigations suggest t

Asymmetric nucleophilic substitution of α-bromo amides via dynamic kinetic resolution for the preparation of dipeptide analogues

Asymmetric nucleophilic substitution reactions of α-bromo α-aryl acetamides derived from L-amino acids are described. The simple and practical syntheses of dipeptide analogues have been developed with dibenzylamine, TBAI and a base to provide 2a-2n and 4