Abstract
The methionine analog, (Z)-L-2-amino-4-methylthio-3-butenoic acid (1) has been synthesized. The key intermediate, (Z)-(±)-methyl 2-acetamido-4-methylthio-3-butenoate (7) was converted to 1 by enantioselective ester hydrolysis using alcalase to give (Z)-L-2-acetamido-4-methylthio-3-butenoic acid (8), followed by enzymatic removal of the N-acetyl group using hog kidney acylase.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
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 call
