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cc-by (c) Paris, Clément et al., 2015
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/67190

Exploiting protected maleimides to modify oligonucleotides, peptides and peptide nucleic acids

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This manuscript reviews the possibilities offered by 2,5-dimethylfuran-protected maleimides. Suitably derivatized building blocks incorporating the exo Diels-Alder cycloadduct can be introduced at any position of oligonucleotides, peptide nucleic acids, peptides and peptoids, making use of standard solid-phase procedures. Maleimide deprotection takes place upon heating, which can be followed by either Michael-type or Diels-Alder click conjugation reactions. However, the one-pot procedure in which maleimide deprotection and conjugation are simultaneously carried out provides the target conjugate more quickly and, more importantly, in better yield. This procedure is compatible with conjugates involving oligonucleotides, peptides and peptide nucleic acids. A variety of cyclic peptides and oligonucleotides can be obtained from peptide and oligonucleotide precursors incorporating protected maleimides and thiols.

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PARIS, Clément, BRUN CUBERO, Omar, PEDROSO MULLER, Enrique, GRANDAS SAGARRA, Anna. Exploiting protected maleimides to modify oligonucleotides, peptides and peptide nucleic acids. _Molecules_. 2015. Vol. 20, núm. 6389-6408. [consulta: 24 de gener de 2026]. ISSN: 1420-3049. [Disponible a: https://hdl.handle.net/2445/67190]

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