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Cyanuric chloride catalyzed Beckmann rearrangement of ketoximein biodegradable ionic liquidss

Academic Article
Publication Date:
2012
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.
Iris type:
01.01 Articolo in rivista
List of contributors:
Maia, Angelamaria
Handle:
https://iris.cnr.it/handle/20.500.14243/75671
Published in:
TETRAHEDRON (OXF., PRINT)
Journal
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