Abstract
Abstract N-Peptidyl-d-glucosamines were synthesized by the stepwise reaction of N-carboxy α-amino acid anhydrides (4-alkyl-2,5-oxazolidinediones) with d-glucosamine hydrochloride in the presence of equimolar sodium methoxide in a mixture of acetonitrile and methanol, or in methanol, at a low temperature. Polymerization reaction of N-carboxy α-amino acid anhydrides (NCAs) did not occur at −50 °C. The mechanism of the reaction was then studied.
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.
