Electrochemically activated CO2 reacts, under mild conditions, with primary and secondary alcohols bearing a leaving group at the alpha-position affording the corresponding cyclic carbonates in high yields; unsubstituted alcohols are converted, after addition of EtI, into the corresponding unsymmetrical ethyl carbonates in moderate to good yields. Tertiary alcohols and phenols are stable to the reagent. (C) 1997 Published by Elsevier Science Ltd.

Electrochemical activation of carbon dioxide: Synthesis of organic carbonates / Casadei, Maria Antonietta; Inesi, Achille; Leucio, Rossi. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - STAMPA. - 38:20(1997), pp. 3565-3568. [10.1016/s0040-4039(97)00664-3]

Electrochemical activation of carbon dioxide: Synthesis of organic carbonates.

CASADEI, Maria Antonietta;INESI, ACHILLE;
1997

Abstract

Electrochemically activated CO2 reacts, under mild conditions, with primary and secondary alcohols bearing a leaving group at the alpha-position affording the corresponding cyclic carbonates in high yields; unsubstituted alcohols are converted, after addition of EtI, into the corresponding unsymmetrical ethyl carbonates in moderate to good yields. Tertiary alcohols and phenols are stable to the reagent. (C) 1997 Published by Elsevier Science Ltd.
1997
01 Pubblicazione su rivista::01a Articolo in rivista
Electrochemical activation of carbon dioxide: Synthesis of organic carbonates / Casadei, Maria Antonietta; Inesi, Achille; Leucio, Rossi. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - STAMPA. - 38:20(1997), pp. 3565-3568. [10.1016/s0040-4039(97)00664-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/247281
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