Abstract
Two aqueous, one-pot, microwave-assisted methods for the rapid synthesis of N-substituted rhodanines from amine substrates are described. Alkyl- and benzylamines could be converted into the corresponding rhodanines with an atom-efficient one-pot, three-step protocol based on carbon disulfide and chloroacetic acid in short reaction times and good to excellent yields. An alternative, microwave-assisted one-pot, one-step protocol using bis(carboxymethyl)trithiocarbonate in water was developed for the synthesis of N-arylrhodanines from anilines.
| Original language | English |
|---|---|
| Pages (from-to) | 5197-5201 |
| Number of pages | 5 |
| Journal | Tetrahedron Letters |
| Volume | 53 |
| Issue number | 39 |
| DOIs | |
| Publication status | Published - 26 Sept 2012 |
| Externally published | Yes |