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Catalytic oxidative carbonylation of amino moieties to ureas, oxamides, 2-oxazolidinones, and benzoxazolones

Articolo
Data di Pubblicazione:
2015
Citazione:
Catalytic oxidative carbonylation of amino moieties to ureas, oxamides, 2-oxazolidinones, and benzoxazolones / Mancuso, R., Raut, D.S., Della Ca, N., Fini, F., Carfagna, C., Gabriele, B.. - In: CHEMSUSCHEM. - ISSN 1864-5631. - ELETTRONICO. - 8:13(2015), pp. 2204-2211. [10.1002/cssc.201500343]
Abstract:
The direct syntheses of ureas, oxamides, 2-oxazolidinones, and benzoxazolones by the oxidative carbonylation of amines, β-amino alcohols, and 2-aminophenols allows us to obtain high value added molecules, which have a large number of important applications in several fields, from very simple building blocks. We have found that it is possible to perform these transformations using the PdI2/KI catalytic system in an ionic liquid, such as 1-butyl-3-methylimidazolium tetrafluoroborate, as the solvent, the solvent/catalyst system can be recycled several times with only a slight loss of activity, and the product can be recovered easily by crystallization.
Tipologia CRIS:
Articolo su rivista
Keywords:
Amines; Amino alcohols; Carbonylation; Ionic liquids; Palladium; Amines; Amino Alcohols; Aminophenols; Benzoxazoles; Catalysis; Imidazoles; Ionic Liquids; Oxamic Acid; Oxazolidinones; Oxidation-Reduction; Palladium; Urea; Chemical Engineering (all); Energy (all); Environmental Chemistry; Materials Science (all); Medicine (all)
Elenco autori:
Mancuso, Raffaella; Raut, Dnyaneshwar S.; Della Ca, Nicola; Fini, Francesco; Carfagna, Carla; Gabriele, Bartolo
Autori di Ateneo:
FINI Francesco
Link alla scheda completa:
https://iris.unimore.it/handle/11380/1123846
Link al Full Text:
https://iris.unimore.it//retrieve/handle/11380/1123846/411405/Fini_F%20-%20Pre_print%20chemsuschem%202015.pdf
Pubblicato in:
CHEMSUSCHEM
Journal
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URL

http://onlinelibrary.wiley.com/doi/10.1002/cssc.201500343/abstract
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