ArticleJournal of the American Chemical Society2022
Regiodivergent Electrophotocatalytic Aminooxygenation of Aryl Olefins.
Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 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.
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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.
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Who cites it
8 citing papers in PubMed.
- Combining Ag(II) and Ag(I) Reactivity Enables Electrophotochemical Acyl Fluoride Installation on (Hetero)Arenes.Journal of the American Chemical Society · 2026Article
- Polyoxygenative functionalization of strained cyclic amides.Nature chemistry · 2026Article
- Excited Organic Radicals in Photoredox Catalysis.JACS Au · 2025Review
- Strategies for AccessingMolecules (Basel, Switzerland) · 2024Review
- Electrophotocatalytic hydrogenation of imines and reductive functionalization of aryl halides.Nature communications · 2024Article
- Photoelectrochemical oxidative C(spNature communications · 2023Article
- Shining Fresh Light on Complex Photoredox Mechanisms through Isolation of Intermediate Radical Anions.ACS catalysis · 2023Article
- Photoredox catalysis harvesting multiple photon or electrochemical energies.Beilstein journal of organic chemistry · 2023Review
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
A method for the regiodivergent aminooxygenation of aryl olefins under electrophotocatalytic conditions is described. The procedure employs a trisaminocyclopropenium (TAC) ion catalyst with visible light irradiation under a controlled electrochemical potential to convert aryl olefins to the corresponding oxazolines with high chemo- and diastereoselectivity. With the judicious choice between two inexpensive and abundant reagents, namely water and urethane, either 2-amino-1-ol or 1-amino-2-ol derivatives could be prepared from the same substrate. This method is amenable to multigram synthesis of the oxazoline products with low catalyst loadings.
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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.