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Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin.
Affiliation:1. Biomolecular NMR Laboratory, Department of Biotechnology, University of Verona, Ca'' Vignal 1, Strada Le Grazie 15, 37134 Verona, Italy;2. Biocrystallography Laboratory, Department of Biotechnology, University of Verona, Ca'' Vignal 1, Strada Le Grazie 15, 37134 Verona, Italy
Abstract:A trialkoxy-diphenyl-methylester and amide linkage for solid-phase peptide synthesis with Fmoc strategy is described. Protected peptide esters can be smoothly cleaved with weak acid, resulting in fragments with intact side-chain protection. Mild acidic cleavage of the corresponding peptide amide resins yields peptide amides.
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