In title cycloadditions microwave irradiation improves product yields and reduces dramatically reaction times in comparison with classical heating with and without refluxing solvents. In the double cycloaddition of nitrile oxides to anthracene a selectivity in favour of unsymmetrical bis-cycloadduct is observed.

1,3-dipolar cycloadditions of polycyclic aromatic hydrocarbons with nitrile oxides under microwave irradiation in the absence of solvent

CHIACCHIO, Ugo;PISTARA', Venerando
1997

Abstract

In title cycloadditions microwave irradiation improves product yields and reduces dramatically reaction times in comparison with classical heating with and without refluxing solvents. In the double cycloaddition of nitrile oxides to anthracene a selectivity in favour of unsymmetrical bis-cycloadduct is observed.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11769/12274
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