A convenient synthesis of (S)- and (R)-4-vinyl oxazolidin-2-one 1 and 2 from the same inexpensive starting material, D-isoascorbic acid, is described. The title compounds were obtained in 44% and 38% yield, respectively, by operationally simple steps. This approach is a suitable alternative to the literature methods and enhances the synthetic utility of these intermediates. Inc.

Synthesis of both enantiomers of 4-vinyl oxazolidin-2-one from a single precursor: D-isoascorbic acid / G., DELLE MONACHE; Misiti, Domenico; P., Salvatore; G., Zappia. - In: CHIRALITY. - ISSN 0899-0042. - STAMPA. - 127:(2000), pp. 143-148. [10.1002/(SICI)1520-636X(2000)12:3<143::AID-CHIR7>3.0.CO;2-3]

Synthesis of both enantiomers of 4-vinyl oxazolidin-2-one from a single precursor: D-isoascorbic acid

MISITI, Domenico;
2000

Abstract

A convenient synthesis of (S)- and (R)-4-vinyl oxazolidin-2-one 1 and 2 from the same inexpensive starting material, D-isoascorbic acid, is described. The title compounds were obtained in 44% and 38% yield, respectively, by operationally simple steps. This approach is a suitable alternative to the literature methods and enhances the synthetic utility of these intermediates. Inc.
2000
D-isoascorbic acid; chiral 4-vinyl oxazolidin-2-ones; chiral heterocycles
01 Pubblicazione su rivista::01a Articolo in rivista
Synthesis of both enantiomers of 4-vinyl oxazolidin-2-one from a single precursor: D-isoascorbic acid / G., DELLE MONACHE; Misiti, Domenico; P., Salvatore; G., Zappia. - In: CHIRALITY. - ISSN 0899-0042. - STAMPA. - 127:(2000), pp. 143-148. [10.1002/(SICI)1520-636X(2000)12:3<143::AID-CHIR7>3.0.CO;2-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/8613
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