S‑Aroylthiooximes: A Facile Route to Hydrogen Sulfide Releasing Compounds with Structure-Dependent Release Kinetics

We report the facile preparation of a family of S-aroylthiooxime (SATO) H2S donors, which are synthesized via a click reaction analogous to oxime formation between S-aroylthio­hydroxyl­amines (SATHAs) and aldehydes or ketones. Analysis of cysteine-triggered H2S release revealed structure-dependent r...

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Veröffentlicht in:Organic letters 2014-03, Vol.16 (6), p.1558-1561
Hauptverfasser: Foster, Jeffrey C, Powell, Chadwick R, Radzinski, Scott C, Matson, John B
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Sprache:eng
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