Julia Ordóñez, Adrian J. Brenes Rucinski, Ciro Romano, Ruben Martin
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Catalytic Deoxygenation of Unactivated 1,2-Diol Motifs via Light-Induced Spin-Center Shift
Herein, we report a light-induced strategy that enables catalytic deoxygenation of unactivated aliphatic 1,2-diol derivatives via a spin-center shift (SCS) manifold. Divergent reactivity can be accomplished depending on the nature of the alkyl radical intermediate. Specifically, secondary alcohols result in α-deoxygenated ketones, whereas a tandem C–C bond-formation/spin-center shift can be promoted with primary alcohols instead in the presence of an appropriate radical acceptor, thus offering an unrecognized opportunity in the SCS arena for repurposing readily available, unactivated 1,2-diol derivatives.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.