An α-aminoglycine derivative suitable for solid phase peptide synthesis using Fmoc strategy

Article abstract of DOI:10.1016/S0040-4039(00)79247-1

α-Boc-amino-Fmoc-glycine was prepared in two steps either from t-butyl carbamate of from 9-fluorenyl-methylcarbamate and used in Solid Phase Peptide Synthesis to prepare α-aminoglycine-containing peptides.