Fluorescent Signaling of Oxone by Desulfurization of Thioamide
Organic Letters2010Vol. 13(3), pp. 370–373
Citations Over TimeTop 21% of 2010 papers
Abstract
The chemosignaling of the oxidant Oxone by selective desulfurization of a thioamide was investigated. Pyrene-thioamide was efficiently converted to its amide analogue by reaction with Oxone, resulting in a pronounced fluorescent turn-on type signaling. Selective signaling of Oxone in aqueous solution was possible in the presence of representative alkali and alkaline earth metal ions, as well as common anions.
Related Papers
- → Structural impact of thioamide incorporation into a β-hairpin(2022)13 cited
- → Preference of cis-Thioamide Structure in N-Thioacyl-N-methylanilines(2020)19 cited
- → über die Struktur der Thioamide und ihrer Derivate, VII Acidität aromatisch substituierter Thioamide(1969)29 cited
- → Selective modification of bifunctional heterocyclic compounds containing amino and thioamide groups in acetic acid medium(2008)3 cited
- → Thioamide Effects on Protein Structure(2019)