: Hydrogenation reactions are staple transformations commonly used across scientific fields to synthesise pharmaceuticals, natural products, and various functional materials. However, the vast majority of these reactions require the use of a toxic and costly catalyst leading to unpractical, hazardous and often functionally limited conditions. Herein, we report a new, general, practical, efficient, mild and high-yielding hydrogen-free electrochemical method for the reduction of alkene, alkyne, nitro and azido groups. Finally, this method has been applied to deuterium labelling.
eHydrogenation: Hydrogen‐free Electrochemical Hydrogenation / Russo, C., Leech, M.C., Walsh, J.M., Higham, J.I., Giannessi, L., Lambert, E., Kiaku, C., Poole, D.L., Mason, J., Goodall, C.A.I., Devo, P., Giustiniano, M., Radi, M., Lam, K.. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - 62:38(2023), p. e202309563. [10.1002/anie.202309563]
eHydrogenation: Hydrogen‐free Electrochemical Hydrogenation
Russo, Camilla;Giustiniano, Mariateresa;
2023
Abstract
: Hydrogenation reactions are staple transformations commonly used across scientific fields to synthesise pharmaceuticals, natural products, and various functional materials. However, the vast majority of these reactions require the use of a toxic and costly catalyst leading to unpractical, hazardous and often functionally limited conditions. Herein, we report a new, general, practical, efficient, mild and high-yielding hydrogen-free electrochemical method for the reduction of alkene, alkyne, nitro and azido groups. Finally, this method has been applied to deuterium labelling.| File | Dimensione | Formato | |
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