256664-48-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 128726-45-4 (S)-2-aminoadipic acid diethyl ester 
• 7425-53-8 ethyl 4-iodobutyrate 
• 134746-23-9 ethyl 2-(((benzyloxy)carbonyl)amino)-2-chloroacetate 
• 104089-17-0 ethyl 4-(iodozincio)butanoate 
• 621-84-1 O-benzyl carbamate 
• 1118-90-7 L-homoglutamic acid 

Relevant academic research and scientific papers

Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling

Interest in unnatural α-Amino acids has increased rapidly in recent years in areas ranging from protein design to medicinal chemistry to materials science. Consequently, the development of efficient, versatile, and straightforward methods for their enanti

Regioselective lipase-catalysed amidation of dicarboxylic N-blocked amino acid diesters - Effect of the side-chain length

Diethyl esters of both (R)- and (S)-N-blocked α-aminoadipic and α- aminopimelic acids yield exclusively the ω-monoamide when they are subjected to amidation catalysed by the lipase B of Candida antarctica in anhydrous diisopropyl ether. These results are