Title of article :
Mild, convenient and versatile Cu-mediated synthesis of N-aryl-2-imidazolidinones
Author/Authors :
Stabile، نويسنده , , Paolo and Lamonica، نويسنده , , Alessandro and Ribecai، نويسنده , , Arianna and Castoldi، نويسنده , , Damiano and Guercio، نويسنده , , Giuseppe and Curcuruto، نويسنده , , Ornella، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2010
Pages :
4
From page :
3232
To page :
3235
Abstract :
A mild, general, convenient and practical methodology for the selective copper-mediated mono N-arylation of unprotected 2-imidazolidinone was developed. Strong electron-donating groups and free hydroxy and amino groups on the aryl iodide substrates were well tolerated. The use of n-butanol as the solvent for the copper-catalysed mono-arylation of 2-imidazolidinone is unprecedented.
Keywords :
Goldberg reaction , Copper catalysis , n-Butanol , N-aryl-2-imidazolidinones
Journal title :
Tetrahedron Letters
Serial Year :
2010
Journal title :
Tetrahedron Letters
Record number :
1872363
Link To Document :
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