| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5221509 | Tetrahedron | 2012 | 4 Pages |
Abstract
Imidazolium-based ionic liquids (ILs) containing ester moieties in the side chain were successfully used as an alternative to traditional ILs in the Beckmann rearrangement of ketoximes catalyzed by 2,4,6-trichloro[1,3,5]triazine. The procedure is mild and suitable for both aromatic and cycloaliphatic substrates affording the rearrangement products in good to quantitative yields. The process is eco-sustainable since these ILs are biodegradable and in addition they can be recovered and reused.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Angelamaria Maia, Domenico C.M. Albanese, Dario Landini,