Abstract
Esters, carbonates, thiocarbonates and carbamates of p-hydroxybenzylcarbonylglycine have been prepared. Free glycine is regenerated in weak alkaline medium by hydrolysis of the acyloxy group followed by an 1–6 elimination. Generally, these compounds are more stable than Z-glycine in trifluoroacetic acid. A series of protected aminoacids and dipeptides has been prepared too. Dilute soda or hydrogen peroxide in ammonia rapidly cleave the protecting group.
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.
