Photodriven Sm-Catalyzed Asymmetric Ketyl-Olefin Coupling
Abstract
High Resolution Image Download MS PowerPoint Slide SmI 2 is a privileged, single-electron reductant employed in the synthesis of diverse products. Though traditionally used in (super)stoichiometric amounts, SmI 2 has recently been employed catalytically with viable turnover strategies. Enantioselective reductive cross-coupling reactions mediated by SmI 2 are scarce and asymmetric methods that use catalytic quantities of SmI 2 are unknown. Herein, we report an enantioselective ketyl-olefin coupling, employing a SmI 2 -derived catalyst with a widely available chiral pyridine-bis(oxazoline) (PyBOX) ligand and a commercially available Ir photocatalyst. A combination of optical, electrochemical, and computational data reveals that a Sm-stabilized PyBOX radical is the reactive species responsible for initiating the reductive coupling step.
Fields of Study & Subjects
Radical Photochemical Reactions
Asymmetric Hydrogenation and Catalysis
Cyclopropane Reaction Mechanisms
Publication details
- Journal / source
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Volume
- 148
- Issue
- 10
- Pages
- 10828–10834
- Publication date
- 4 March 2026
- Language
- EN