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. - ISSN 1521-3773. - 62:38(2023). [10.1002/anie.202309563]
eHydrogenation: Hydrogen-free Electrochemical Hydrogenation
Giannessi, Lisa;Radi, Marco;
2023-01-01
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.