ArticleOrganic letters2019
Iron-Catalyzed Hydroamination and Hydroetherification of Unactivated Alkenes.
Article in Organic letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 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
5 citing papers in PubMed.
- Intermolecular Anti-Markovnikov Hydroamination of Alkenes with Sulfonamides, Sulfamides, and Sulfamates.ACS catalysis · 2024Article
- Iron Trichloride-Mediated Cascade Reaction of Aminosugar Derivatives for the Synthesis of Fused Tetrahydroisoquinoline-Tetrahydrofuran Systems.ACS omega · 2022Article
- Development of highly efficient platinum catalysts for hydroalkoxylation and hydroamination of unactivated alkenes.Nature communications · 2021Article
- Catalytic Hydroetherification of Unactivated Alkenes Enabled by Proton-Coupled Electron Transfer.Angewandte Chemie (International ed. in English) · 2020Article
- Synthesis of Tetrahydroisoquinolines Through an Iron-Catalyzed Cascade: Tandem Alcohol Substitution and Hydroamination.Organic letters · 2019Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
The hydrofunctionalization of alkenes, explored for over 100 years, offers the potential for a direct, atom-economical approach to value-added products. While thermodynamically favored, the kinetic barrier to such processes necessitates the use of catalysts to control selectivity and reactivity. Modern variants typically rely on noble metals that require different ligands for each class of hydrofunctionalization, thereby limiting generality. This Letter describes a general iron-based system that catalyzes the hydroamination and hydroetherification of simple unactivated olefins.
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Registered trials
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