Sequential 1,3-Dipolar Cycloaddition of Nitrones to β-(2-Aminophenyl) α,β-Ynones and Cyclocondensation: A New Entry to the Isoxazolino[4,5-c]quinoline Ring

Abbiati, G; Marinelli, Fabio; Rossi, E; Verdecchia, M.; Arcadi, Antonio

doi:10.1002/ejoc.200800994

The reaction of β-(2-aminophenyl) α,β-ynones with N-methyl nitrones provides a simple and efficient entry to the isoxazolino[ 4,5-c]quinoline ring system through a sequential 1,3-dipolar cycloaddition/annulation process.

Titolo:	Sequential 1,3-Dipolar Cycloaddition of Nitrones to β-(2-Aminophenyl) α,β-Ynones and Cyclocondensation: A New Entry to the Isoxazolino[4,5-c]quinoline Ring
Autori:	ABBIATI G MARINELLI, Fabio ROSSI E VERDECCHIA M. ARCADI, Antonio mostra contributor esterni nascondi contributor esterni
Data di pubblicazione:	2009
Rivista:	EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Abstract:	The reaction of β-(2-aminophenyl) α,β-ynones with N-methyl nitrones provides a simple and efficient entry to the isoxazolino[ 4,5-c]quinoline ring system through a sequential 1,3-dipolar cycloaddition/annulation process.
Handle:	http://hdl.handle.net/11697/12926
Appare nelle tipologie:	1.1 Articolo in rivista

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