A novel mechanochemical approach is described for chloride-templated head-to-tail macrocyclization of a pentapeptide and a hexapeptide. This straightforward method allows the solvent-free preparation of cyclopeptides with yields comparable to solution-based approaches without the need for high dilution of the reaction mixture and with significantly reduced reaction times and organic waste amount.

Rapid and Green Anion-Assisted Mechanochemical Peptide Cyclization / M. Duvnjak, N. Vidović, K. Užarević, G. Horvat, V. Tomišić, G. Speranza, N. Cindro. - In: ACS SUSTAINABLE CHEMISTRY & ENGINEERING. - ISSN 2168-0485. - 13:1(2025 Jan 03), pp. 30-35. [10.1021/acssuschemeng.4c03309]

Rapid and Green Anion-Assisted Mechanochemical Peptide Cyclization

G. Speranza
Penultimo
;
2025

Abstract

A novel mechanochemical approach is described for chloride-templated head-to-tail macrocyclization of a pentapeptide and a hexapeptide. This straightforward method allows the solvent-free preparation of cyclopeptides with yields comparable to solution-based approaches without the need for high dilution of the reaction mixture and with significantly reduced reaction times and organic waste amount.
ball-milling; cyclization; green chemistry; peptides and proteins; solvent-free
Settore CHEM-05/A - Chimica organica
3-gen-2025
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1157543
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