: 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, Camilla; Leech, Matthew C.; Walsh, Jamie M.; Higham, Joe I.; Giannessi, Lisa; Lambert, Emmanuelle; Kiaku, Cyrille; Poole, Darren L.; Mason, Joseph; Goodall, Charles A. I.; Devo, Perry; Giustiniano, Mariateresa; Radi, Marco; Lam, Kevin. - 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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