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.

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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

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article

Photocatalytic deoxygenative Z-selective olefination of aliphatic alcohols

Irene Sánchez‐Sordo, Emanuele Azzi, Sai Rohini Narayanan Kolusu, Manuel Nappi et al.
8 citations
Nature Communications
Radical Photochemical Reactions
7.49
article

Photocatalytic deoxygenative Z-selective olefination of aliphatic alcohols

Irene Sánchez‐Sordo, Emanuele Azzi, Sai Rohini Narayanan Kolusu, Manuel Nappi, Carla Aira-Rodríguez
article en
8 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
Universidade de Santiago de Compostela (ES), Center for Research in Molecular Medicine and Chronic Diseases (ES)
European Commission, Xunta de Galicia, European Regional Development Fund, Agencia Estatal de Investigación
Clean water and sanitation
Openalex Percentile: Top 3%
Radical Photochemical Reactions
7.49
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