The reaction between aliphatic amines and propylene carbonate can be performed in solventless conditions under microwave irradiation, becoming nearly complete within 15 min of irradiation. Oxidation of the formed mixture of 2-hydroxyethylcarbamates gives 3,5-methylalkyl-oxazolidine-2,4-diones. These compounds can react further with aliphatic primary amines to give N-lactoylureas.

Galliani, G., Rindone, B., Saliu, F., Bertoa, R., Terraneo, A. (2009). ORGN 230-Reaction of a 1,3-oxazolidine-2,4-dione with carbon nucleophiles [Altro].

ORGN 230-Reaction of a 1,3-oxazolidine-2,4-dione with carbon nucleophiles

Galliani, G;Rindone, B;Saliu, F;
2009

Abstract

The reaction between aliphatic amines and propylene carbonate can be performed in solventless conditions under microwave irradiation, becoming nearly complete within 15 min of irradiation. Oxidation of the formed mixture of 2-hydroxyethylcarbamates gives 3,5-methylalkyl-oxazolidine-2,4-diones. These compounds can react further with aliphatic primary amines to give N-lactoylureas.
Altro
Scientifica
3,5-Dialkyl-oxazolidine-2,4-diones; N-lactoyl-N,N0-dialkylureas; solventless reaction
English
Galliani, G., Rindone, B., Saliu, F., Bertoa, R., Terraneo, A. (2009). ORGN 230-Reaction of a 1,3-oxazolidine-2,4-dione with carbon nucleophiles [Altro].
Galliani, G; Rindone, B; Saliu, F; Bertoa, R; Terraneo, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/36132
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