Abstract

Solid-phase synthesis of an O-palmitoylated peptide has been achieved by either palmitoylation of the resin-bound peptide or synthesis of palmitoylated Fmoc-Thr and subsequent solid-phase incorporation. The desired peptides containing palmitoylated Thr were isolated by reversed-phase C 18 HPLC. An O → N acyl shift was encountered when palmitoylated Fmoc-Thr was utilized.

Full Text
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

Disclaimer: 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.