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Suppression of alpha-carbon racemization in peptide synthesis based on a thiol-labile amino protecting group | Nature Communications
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SOLVED: Fmoc-Cl is a common protecting group for amino acids. What other problem might arise with this amino acid during peptide synthesis?
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Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups | Nature Communications
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Selective Deprotection of N-Boc-Protected tert-Butyl Ester Amino Acids by the CeCl3*7H20-NaI System in Acetonitrile
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Molecules | Free Full-Text | Efficient Fmoc-Protected Amino Ester Hydrolysis Using Green Calcium(II) Iodide as a Protective Agent
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