Leveraging electrochemistry, a new synthesis of non-natural derivatives of itaconic acid is proposed by utilizing carbon dioxide (CO2) as a valuable C1 synthon. An electrochemical cross-electrophile coupling between allenoates and CO2 was targeted, allowing for the synthesis of both mono- and di- carboxylation products in a catalyst- and additive-free environ- ment (yields up to 87 %, 30 examples). Elaboration of the model mono-carboxylation product, and detailed cyclovoltammetric, as well as mechanistic analyses complete the present investigation.

Andrea Brunetti, M.G. (2024). Electrochemical Synthesis of Itaconic Acid Derivatives via Chemodivergent Single and Double Carboxylation of Allenes with CO2. CHEMISTRY-A EUROPEAN JOURNAL, 30(49), 1-7 [10.1002/chem.202401754].

Electrochemical Synthesis of Itaconic Acid Derivatives via Chemodivergent Single and Double Carboxylation of Allenes with CO2

Andrea Brunetti;Mauro Garbini;Giuseppe Autuori;Giulio Bertuzzi
;
Marco Bandini
Conceptualization
2024

Abstract

Leveraging electrochemistry, a new synthesis of non-natural derivatives of itaconic acid is proposed by utilizing carbon dioxide (CO2) as a valuable C1 synthon. An electrochemical cross-electrophile coupling between allenoates and CO2 was targeted, allowing for the synthesis of both mono- and di- carboxylation products in a catalyst- and additive-free environ- ment (yields up to 87 %, 30 examples). Elaboration of the model mono-carboxylation product, and detailed cyclovoltammetric, as well as mechanistic analyses complete the present investigation.
2024
Andrea Brunetti, M.G. (2024). Electrochemical Synthesis of Itaconic Acid Derivatives via Chemodivergent Single and Double Carboxylation of Allenes with CO2. CHEMISTRY-A EUROPEAN JOURNAL, 30(49), 1-7 [10.1002/chem.202401754].
Andrea Brunetti, Mauro Garbini, Giuseppe Autuori, Chiara Zanardi, Giulio Bertuzzi, Marco Bandini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/996211
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