Thiazolidine chemistry revisited: a fast, efficient and stable click-type reaction at physiological pH.

Autor: Bermejo-Velasco D; Translational Chemical Biology Laboratory, Division of Polymer Chemistry, Department of Chemistry-Ångstrom, Uppsala University, Uppsala, Sweden. oommen.varghese@kemi.uu.se., Nawale GN, Oommen OP, Hilborn J, Varghese OP
Jazyk: angličtina
Zdroj: Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2018 Nov 01; Vol. 54 (88), pp. 12507-12510.
DOI: 10.1039/c8cc05405c
Abstrakt: We describe the fast reaction kinetics between 1,2-aminothiols and aldehydes. Under physiological conditions such a click-type reaction afforded a thiazolidine product that remains stable and did not require any catalyst. This type of bioorthogonal reaction offers enormous potential for the coupling of biomolecules in an efficient and biocompatible manner.
Databáze: MEDLINE