Demonstrates effective synthesis of thiazolidine-2-thiones, indicating a practical chemical method.
A rapid and practical approach for the synthesis of trifluoromethyl‐substituted thiazolidine‐2‐thiones through [3 + 2] annulation of dithiocarbamate salts with CF 3 ‐imidoyl sulfoxonium ylides (TFISYs) under catalyst‐, oxidant‐, and additive‐free conditions. The transformation features simple operation, environmentally benign, very mild conditions, readily available reactants, high efficiency, and scalability, providing a facile and straightforward entry to biologically valuable N , S ‐containing heterocycle molecules.
No takes yet. Share an insight, caveat, or question.
Han et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: