Allylic amination of unfunctionalized olefins by nitroarenes and CO, catalyzed by Ru3(CO)12/Ph-BIAN (Ph-BIAN = bis(phenylimino)acenaphthenequinone) : extension to the synthesis of allylic amines with strongly electron-withdrawing or electron-donating groups on the aryl ring
Articolo
Data di Pubblicazione:
2004
Citazione:
Allylic amination of unfunctionalized olefins by nitroarenes and CO, catalyzed by Ru3(CO)12/Ph-BIAN (Ph-BIAN = bis(phenylimino)acenaphthenequinone) : extension to the synthesis of allylic amines with strongly electron-withdrawing or electron-donating groups on the aryl ring / F.A.C. Ragaini, S. Cenini, F. Turra, A. Caselli. - In: TETRAHEDRON. - ISSN 0040-4020. - 60:23(2004 May 31), pp. 4989-4994.
Abstract:
The allylic amination of unfunctionalyzed olefins by nitroarenes under CO pressure, catalyzed by Ru3(CO)12/Ph-BIAN
(Ph-BIAN = bis(phenylimino)acenaphthenequinone) has been extended to some substrates with strongly electron-withdrawing groups on the nitroarene. Reaction of 1,4-dinitrobenzene selectively affords functionalization of only one nitro group, the other remaining unreacted.
However, the second nitro group can be reduced in one pot by CO/H2O in the presence of the same catalytic system employed in the
amination reaction, to afford the corresponding 4-amino derivative. Some attempts to render the reaction enantioselective by employing chiral bis-oxazolines as ligands in place of Ph-BIAN are described. Bis-oxazolines are suitable ligands for the reaction, although not as
efficient as Ph-BIAN, but the allylic amine obtained was found to be racemic.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Allylic amines; Carbonylation reactions; Imines; Nitroarenes; Ruthenium
Elenco autori:
F.A.C. Ragaini, S. Cenini, F. Turra, A. Caselli
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