80887-22-5

Upstream product

• 103-63-9 1-phenyl-2-bromoethane 
• 1068-90-2 2-acetylaminomalonic acid diethyl ester 
• 5463-92-3 2-acetylamino-2-phenylethylmalonic acid diethyl ester 

Downstream Products

• 27038-09-1 (2S)-2-amino-4-phenyl-1-butanol 
• 60425-49-2 (+)-α-amino-4-phenylbutyric acid methyl ester hydrochloride 
• 105382-09-0 L-(+)-homophenylalanine hydrochloride 
• 96613-91-1 (R)-2-Acetamido-4-phenylbutansaeure 
• 141289-30-7 N-acetyl-DL-homophenylalanine ethyl ester 

Relevant academic research and scientific papers

Concise synthesis and enzymatic resolution of L-(+)-homophenylalanine hydrochloride

The N-acetyl-homophenylalanine ethyl ester was synthesized by a simple three-step-reaction strategy. L-(+)-homophenylalanine hydrochloride with 98% ee was obtained through a kinetic resolution process using industrial enzyme alcalase. Compared with other

Variations of the Nature of the Chiral Auxiliary with a Highly Enantioselective Chiral NADH Model

Various chiral amine alcohols have been used as chiral auxiliares for a highly enantioselective NADH model.Some of these are new reagents which have been obtained by an enzymic resolution method.