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Updated: May 22, 2026

Solid Phase Synthesis of a Functionalized Bis-Peptide Using "Safety Catch" Methodology
Published on: May 15, 2012
A general solid phase method for the synthesis of sequence independent peptidyl-fluoromethyl ketones
Gheorghe-Doru Roiban1, Mihaela Matache, Niculina D Hădade
1Department of Chemistry, Marie Curie Excellence Team, Technical University München, 4 Lichtenberg str. 85748, Garching, Germany.
Abstract:
We present here a new, general, solid phase strategy for the synthesis of sequence independent peptidyl-fluoromethyl ketones using standard Fmoc peptide chemistry. Our method is based on the synthesis of bifunctional linkers which allows the incorporation of amino acid fluoromethyl ketone unit at the C-terminal end of peptide sequences. Application of this approach for the synthesis of activity based probes for SENPs is also described.
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