Abstract
Abstract A new and convenient method for the preparation of pure enantiomers of α-amino acids is described. Industrial papain, catalyzes the synthesis of L-Z-amino acid ethyl esters in ethanolic medium, with good yields. These esters are obtained from DL-Z-amino acids with 100% optical purity. Unreactive D-Z-amino acids are readily isolated from reaction medium. Physical constants of natural and xenobiotic L-Z-amino acid esters and D-Z-amino acids are described.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
