ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022
Electrochemistry and Reactivity of Chelation-stabilized Hypervalent Bromine(III) Compounds.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 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.
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.
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Who cites it
8 citing papers in PubMed.
- Electrochemistry of Hypervalent Halogen Compounds.Accounts of chemical research · 2026Article
- Electrochemical synthesis of cyclic biaryl λBeilstein journal of organic chemistry · 2025Article
- Highly Acidic Electron-Rich Brønsted Acids Accelerate Asymmetric Pictet-Spengler Reactions by Virtue of Stabilizing Cation-π Interactions.Journal of the American Chemical Society · 2024Article
- Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities.Chemical science · 2024Review
- Electrochemical Synthesis of Dimeric λOrganic letters · 2023Article
- Multifunctional Organocatalysts - Singly-Linked and Macrocyclic Bisphosphoric Acids for Asymmetric Phase-Transfer and Brønsted-Acid Catalysis.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- Iodine-Iodine Cooperation Enables Metal-Free C-N Bond-Forming Electrocatalysis via Isolable Iodanyl Radicals.Journal of the American Chemical Society · 2022Article
- Electrochemistry and Reactivity of Chelation-stabilized Hypervalent Bromine(III) Compounds.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
Hypervalent bromine(III) reagents possess a higher electrophilicity and a stronger oxidizing power compared to their iodine(III) counterparts. Despite the superior reactivity, bromine(III) reagents have a reputation of hard-to-control and difficult-to-synthesize compounds. This is partly due to their low stability, and partly because their synthesis typically relies on the use of the toxic and highly reactive BrF
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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.