1598416-01-3Relevant academic research and scientific papers
A facile Fmoc solid phase synthesis strategy to access epimerization-prone biosynthetic intermediates of glycopeptide antibiotics
Brieke, Clara,Cryle, Max J.
supporting information, p. 2454 - 2457 (2014/05/20)
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and teicoplanin-type peptides is described. Epimerization of highly racemization-prone arlyglycine derivatives is suppressed through optimized Fmoc-deprotection
