The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrrolidone electro- generated base allowed to establish a new methodology for the synthesis of oxazolidin-2-ones. Chiral oxazolidin- 2-ones (Evans' chiral auxiliaries) were obtained in good to high yields avoiding the use of toxic, polluting or dangerous reagents. This methodology represents a further example of the direct employment of carbon dioxide as a source of carbon in organic synthesis.

Sotgiu, G., CASADEI M., A., Feroci, M., Inesi, A., Rossi, L. (2000). The Reaction of 1,2-amino alcohols with carbon dioxide in the presence of 2-pyrrolidone electrogenerated base. New synthesis of chiral oxazolidin-2-ones. JOURNAL OF ORGANIC CHEMISTRY, 65(15), 4759-4761 [10.1021/jo0002386].

The Reaction of 1,2-amino alcohols with carbon dioxide in the presence of 2-pyrrolidone electrogenerated base. New synthesis of chiral oxazolidin-2-ones

SOTGIU, Giovanni;
2000-01-01

Abstract

The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrrolidone electro- generated base allowed to establish a new methodology for the synthesis of oxazolidin-2-ones. Chiral oxazolidin- 2-ones (Evans' chiral auxiliaries) were obtained in good to high yields avoiding the use of toxic, polluting or dangerous reagents. This methodology represents a further example of the direct employment of carbon dioxide as a source of carbon in organic synthesis.
2000
Sotgiu, G., CASADEI M., A., Feroci, M., Inesi, A., Rossi, L. (2000). The Reaction of 1,2-amino alcohols with carbon dioxide in the presence of 2-pyrrolidone electrogenerated base. New synthesis of chiral oxazolidin-2-ones. JOURNAL OF ORGANIC CHEMISTRY, 65(15), 4759-4761 [10.1021/jo0002386].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11590/117263
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