Synthesis of water-soluble scaffolds for peptide cyclization, labeling, and ligation

Authors
Publication date 2012
Journal Organic Letters
Volume | Issue number 14 | 5
Pages (from-to) 1194-1197
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract The synthesis and applications of water-soluble scaffolds that conformationally constrain side chain unprotected linear peptides containing two cysteines are described. These scaffolds contain a functionality with orthogonal reactivity to be used for labeling and ligation. This is illustrated by the chemical ligation of two dissimilar constrained peptides via oxime ligation or strain-promoted azide-alkyne cycloaddition in aqueous media
Document type Article
Language English
Published at https://doi.org/10.1021/ol203259a
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