Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219073 | Tetrahedron | 2012 | 5 Pages |
Abstract
A base-free, recyclable approach for the conjugate addition of aliphatic nitro compounds to enones to give γ-nitro ketones is presented. Reactions are carried out in an ionic liquid with a basic anionic moiety, such as BmimNTf2, as the solvent, under mild conditions (25 °C for 24 h). The IL medium could be recycled several times without any appreciable loss of activity, after a simple extraction procedure for the separation of the reaction product.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Raffaella Mancuso, Alessandro Palmieri, Roberto Ballini, Bartolo Gabriele,