ArticleAngewandte Chemie (International ed. in English)2022
Electrochemical Fluorination of Vinyl Boronates through Donor-Stabilized Vinyl Carbocation Intermediates.
Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 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
3 citing papers in PubMed.
- One-Pot Synthesis of Terminal Alkynes from Alkenes.JACS Au · 2024Article
- Accessing Medium-Sized Rings via Vinyl Carbocation Intermediates.Organic letters · 2024Article
- Vinyl cation-mediated intramolecular hydroarylation of alkynes using pyridinium reagents.Chemical communications (Cambridge, England) · 2022Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
The electrochemical generation of vinyl carbocations from alkenyl boronic esters and boronates is reported. Using easy-to-handle nucleophilic fluoride reagents, these intermediates are trapped to form fully substituted vinyl fluorides. Mechanistic studies support the formation of dicoordinated carbocations through sequential single-electron oxidation events. Notably, this electrochemical fluorination features fast reaction times and Lewis acid-free conditions. This transformation provides a complementary method to access vinyl fluorides with simple fluoride salts such as TBAF.
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Registered trials
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