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 |
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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 |