Abstract
AbstractThe synthesis of α‐ureidopeptidomimetics employing a simple, mild and straight forward route starting from benzyloxy carbonyl (Cbz‐) protected amino acid esters in presence of 2‐Cl pyridine (2‐chloropyridine) and Tf2O (triflic anhydride) in one‐pot is described. The in situ generated isocyanate intermediates react with amino acid esters to yield the title compounds in good yields (89‐96%) and the protocol proved to be racemization free.
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.
