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. SperanzaPenultimo
;
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.| File | Dimensione | Formato | |
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