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We report here an operationally very simple method to greatly facilitate chemical protein synthesis by fully convergent and one-pot native chemical ligations utilizing the Fluorenylmethyloxycarbonyl (Fmoc) moiety as an N-masking group of the N-terminal cysteine of the middle peptide thioester segment(s). The Fmoc group is stable to harsh oxidative conditions frequently used to generate peptide thioester from hydrazide or o-aminoanilide. The ready availability of the Fmoc-Cys(Trt)-OH, routinely used in Fmoc chemistry solid phase peptide