Abstract

Fmoc-Aib-F shows superior efficiency for the introduction of Aib (α-aminoisobutyric acid) residues into a model peptide containing four adjacent Aib units in comparison with symmetrical anhydrides, UNCA's and activation by PyBroP. The Aib-rich sequence alamethicin acid has also been synthesized via Fmoc amino acid fluorides.

Full Text
Published version (Free)

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