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Simple synthesis and functionalisation of α-hydroxyglycine-containing peptide fragments
Pooja R Solanke1, Debolina Sarkar1, Pranab C Saha1
1Department of Chemistry & Biochemistry, University of Arizona, Tucson, AZ 85721, USA.
None:
We report here a method for the chemical synthesis of Fmoc-protected α-hydroxyglyine (α-OH-Gly) dipeptides. Our method features operational simplicity and is compatible with protecting groups for peptide synthesis. Utility is then demonstrated through substitution at the α-OH-Gly position to yield myriad non-natural amino acid-containing dipeptide fragments.
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