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A Strategy for Thioamide Incorporation During Fmoc Solid-Phase Peptide Synthesis with Robust Stereochemical Integrity
preprintsubmitted on 30.05.2019, 18:10 and posted on 31.05.2019, 15:18 by luis camacho III, Bryan J. Lampkin, Brett VanVeller
We describe a method to protect the sensitive stereochemistry of the thioamide—in analogy to the protection of the functional groups of amino acid side chains—in order to preserve the thioamide moiety during peptide elongation.