ArticleOrganic letters2017
Radical Cation Cycloadditions Using Cleavable Redox Auxiliaries.
Article in Organic letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 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
11 citing papers in PubMed.
- TiOPrecision chemistry · 2026Article
- Deciphering Asymmetric Induction in Photoredox Catalysis by Chiral Counteranions.ACS catalysis · 2026Article
- Comprehensive investigation of long non-coding RNAs in an endophytic fungus Calcarisporium arbuscula NRRL 3705.Archives of microbiology · 2023Article
- Organophotocatalytic [2+2] Cycloaddition of Electron-Deficient Styrenes.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- Article
- Ruthenium-Catalyzed Cycloadditions to Form Five-, Six-, and Seven-Membered Rings.Chemical reviews · 2021Review
- Stereoretention in styrene heterodimerisation promoted by one-electron oxidants.Chemical science · 2020Article
- Effect of Reaction Media on Photosensitized [2+2]-Cycloaddition of Cinnamates.ChemistryOpen · 2020Article
- A Redox Auxiliary Strategy for Pyrrolidine Synthesis via Photocatalytic [3+2] Cycloaddition.Asian journal of organic chemistry · 2019Article
- Discovery and Elucidation of Counteranion Dependence in Photoredox Catalysis.Journal of the American Chemical Society · 2019Article
- Stepwise radical cation Diels-Alder reaction via multiple pathways.Beilstein journal of organic chemistry · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
The incorporation of an easily oxidized arylsulfide moiety facilitates the photocatalytic generation of alkene radical cations that undergo a variety of cycloaddition reactions with electron-rich reaction partners. The sulfide moiety can subsequently be reductively cleaved in a traceless fashion, affording products that are not otherwise directly accessible using photoredox catalysis. This approach constitutes a novel oxidative "redox auxiliary" strategy that offers a practical means to circumvent a fundamental thermodynamic limitation facing photoredox reactions.
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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.