Demonstrates a new multicomponent reaction, yielding diverse 3-iminoisoindoline-1-thiones, suggesting efficient synthesis techniques.
A base‐catalyzed, oxidative multicomponent condensation involving primary anilines, elemental sulfur, and phthalaldehyde is reported. Utilizing readily available starting materials, this protocol affords a novel series of structurally diverse 3‐iminoisoindoline‐1‐thiones in satisfactory yields under mild reaction conditions. Furthermore, the methodology was successfully extended to 1,8‐diaminonaphthalene, yielding the photosensitizer 12 H ‐isoindolo[2,1‐ a ]perimidine‐12‐thione in excellent yields with a simplified purification process via filtration.
No takes yet. Share an insight, caveat, or question.
Nguyen et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: