Title of article :
Trihaloisocyanuric acids as convenient reagents for regioselective halogenation of β-dicarbonyl compounds
Author/Authors :
Mendonça، نويسنده , , Gabriela F. and Sindra، نويسنده , , Haryadylla C. and de Almeida، نويسنده , , Leonardo S. and Esteves، نويسنده , , Pierre M. and de Mattos، نويسنده , , Marcio C.S. de Mattos، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
3
From page :
473
To page :
475
Abstract :
The reaction of β-dicarbonyl compounds (β-ketoesters and β-diketones) with 0.34 mol equiv of trichloro- and tribromoisocyanuric acids produced regioselectively the corresponding α-monohalo β-dicarbonyl compound. On the other hand, utilization of 0.68 mol equiv of the trihaloisocyanuric acid produced the α,α-dihalo β-dicarbonyl compound.
Keywords :
?-diketones , ?-Ketoesters , Halogenation , regioselectivity
Journal title :
Tetrahedron Letters
Serial Year :
2009
Journal title :
Tetrahedron Letters
Record number :
1862419
Link To Document :
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