ArticleChem2025
Reductive Coupling of Acrylamides and Carbonyls via Solvated Electrons from Excited State Acridyl Radicals.
Article in Chem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Mechanistic Diversity in Photoexcited Radical Redox Chemistry: A Critical Evaluation.Angewandte Chemie (International ed. in English) · 2026Review
- Photophysics of Doubly Reduced Quinacridone Dyes: Toward Redox Reactivity Activated by Red Light.Artificial photosynthesis (Washington, D.C.) · 2026Article
- Article
- Photocatalytic Controlled Halodefluorination of Perfluoroalkyl Compounds UsingJournal of the American Chemical Society · 2026Article
- Aldehyde-Olefin Couplings by Photoinduced Reduction of Electron-Deficient Olefins with Hantzsch Ester Anions.Angewandte Chemie (International ed. in English) · 2026Article
- Photochemical reduction of aryl chlorides, bromides, and iodidesChemical science · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
The reductive coupling of carbonyls and alkenes is primarily promoted by super stoichiometric quantities of samarium diiodide (SmI2). This reductant requires fresh preparation under moisture-free anaerobic conditions for successful reactivity. Herein, we describe a new method for reductive coupling of acrylamides with unactivated ketones and aldehydes by employing acridine radicals as excited state reductants. Ultrafast transient absorption spectroscopy experiments provided a clearer picture of the excited state acridine radical and its mechanism of action, which likely proceeds via the formation of solvated electrons in acetonitrile.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.