Photochemical Decatungstate‐Catalyzed Hydroacylation of Maleimides

Succinimides constitute a useful and coveted structural scaffold in organic synthesis, due to their wide range of applications. Herein, we present an efficient approach for the synthesis of substituted succinimides by means of photocatalysis. Namely, tetra n‐butylammonium decatungstate, a well‐known photocatalyst, was employed under light irradiation, in order to synthesize a variety of succinimide ketones via a direct hydroacylation reaction of N ‐substituted maleimides. A diverse range of aldehydes and N ‐substituted maleimides show great compatibility with this protocol, providing functionalized succinimides in satisfactory yields. The protocol is applicable to flow conditions, as well as in a gram scale reaction.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-24
DOI
https://doi.org/10.1002/ejoc.70438
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Photochemical Decatungstate‐Catalyzed Hydroacylation of Maleimides

Christoforos G. Kokotos, Naya A. Stini, Manos V. G. Lantzanakis
European Journal of Organic Chemistry
Radical Photochemical Reactions
article

Photochemical Decatungstate‐Catalyzed Hydroacylation of Maleimides

Christoforos G. Kokotos, Naya A. Stini, Manos V. G. Lantzanakis
article en

Abstract

Succinimides constitute a useful and coveted structural scaffold in organic synthesis, due to their wide range of applications. Herein, we present an efficient approach for the synthesis of substituted succinimides by means of photocatalysis. Namely, tetra n‐butylammonium decatungstate, a well‐known photocatalyst, was employed under light irradiation, in order to synthesize a variety of succinimide ketones via a direct hydroacylation reaction of N ‐substituted maleimides. A diverse range of aldehydes and N ‐substituted maleimides show great compatibility with this protocol, providing functionalized succinimides in satisfactory yields. The protocol is applicable to flow conditions, as well as in a gram scale reaction.

European Journal of Organic Chemistry
National and Kapodistrian University of Athens (GR)
Clean water and sanitation
Openalex Percentile: Top 7%
Radical Photochemical Reactions
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