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.

Electrochemical activation of carbon dioxide: Synthesis of organic carbonates.

ROSSI, LEUCIO
1997-01-01

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.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/17624
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