Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272263 | Tetrahedron Letters | 2012 | 5 Pages |
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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Christoph Nitsche, Christian D. Klein,