Photocatalytic deoxygenative Z-selective olefination of aliphatic alcohols
Alcohols are one of the most abundant functional groups in commercially available materials and biologically active compounds. Herein, we report a metal-free photocatalytic method for the deoxygenative Z-selective olefination of aliphatic alcohols. Key to this methodology is the radical olefination and isomerization of unstabilized open-shell species generated in situ by a catalytic reductive scission of benzoate esters. These processes are simultaneously orchestrated by a single phenothiazine photocatalyst via singlet and triplet excited states. Our protocol is distinguished by its wide substrate scope and broad applicability, even in the context of pharmaceuticals and saccharides. Given the mild and water-compatible conditions, our chemistry can also be utilized to functionalize DNA headpieces for DELs applications.
Authors
- Irene Sánchez‐Sordo (ORCID: https://orcid.org/0000-0001-7471-1831)
- Emanuele Azzi (ORCID: https://orcid.org/0000-0002-2284-2925)
- Sai Rohini Narayanan Kolusu (ORCID: https://orcid.org/0000-0002-5292-8658)
- Manuel Nappi (ORCID: https://orcid.org/0000-0002-3023-0574)
- Carla Aira-Rodríguez (ORCID: https://orcid.org/0000-0003-0763-6290)
Institutions
- Universidade de Santiago de Compostela (ES)
- Center for Research in Molecular Medicine and Chronic Diseases (ES)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-04-02
- DOI
- https://doi.org/10.1038/s41467-025-58469-z
- Citations
- 8
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 7.49
Funders
- European Commission
- Xunta de Galicia
- European Regional Development Fund
- Agencia Estatal de Investigación