Diazabicyclo[5.4.0]undecene (DBU) reacts with carbon dioxide and N-subsititued-2-chloroacetoamides in a very simple one-step procedure, to give the corresponding 3-substituted oxazolidin-2,4-diones in excellent yields.

Galliani, G., Rindone, B., Saliu, F. (2009). Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU). TETRAHEDRON LETTERS, 50(36), 5123-5125 [10.1016/j.tetlet.2009.06.109].

Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU)

RINDONE, BRUNO;SALIU, FRANCESCO
2009

Abstract

Diazabicyclo[5.4.0]undecene (DBU) reacts with carbon dioxide and N-subsititued-2-chloroacetoamides in a very simple one-step procedure, to give the corresponding 3-substituted oxazolidin-2,4-diones in excellent yields.
Articolo in rivista - Articolo scientifico
3-Alkyloxazolidin-2,4-diones; Carbon dioxide; DBU; Amines; Chemical synthesis
English
5123
5125
Galliani, G., Rindone, B., Saliu, F. (2009). Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU). TETRAHEDRON LETTERS, 50(36), 5123-5125 [10.1016/j.tetlet.2009.06.109].
Galliani, G; Rindone, B; Saliu, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/9108
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