ArticleAngewandte Chemie (International ed. in English)2021
Rules of Nucleophilic Additions to Zigzag Nanographene Diones*.
Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- π-Radical Cascades to Peri-Fused Triangulene Dimers.Angewandte Chemie (International ed. in English) · 2026Article
- A Potassium Base-Promoted Intramolecular Enolate-Olefin Metathesis.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Achieving Olympicene Functionalization Three Ways.The Journal of organic chemistry · 2025Article
- Carbonyl mediated fluorescence in aceno[Chemical science · 2024Article
- The taming of Clar's hydrocarbon.Chemical communications (Cambridge, England) · 2022Review
- Subphthalocyanine-triangulene dyads: Property tuning for light-harvesting device applications.Energy science & engineering · 2022Article
- Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon.Chemical communications (Cambridge, England) · 2022Article
- Rules of Nucleophilic Additions to Zigzag Nanographene Diones*.Angewandte Chemie (International ed. in English) · 2021Article
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4 authors.
Funding
Abstract
Nucleophilic addition of carbon-centered nucleophiles to nanographene ketones represents a valuable late-stage method for the functionalization of zigzag nanographenes, but its use is rare in the chemical literature. Using two model systems, non-Kekulé triangulene-4,8-dione and Kekulé anthanthrone, we identify unexpected regioselectivities and uncover the rules that govern these reactions. Considering the large number of nanographene ketones that have been reported since the pioneering work of Eric Clar, this method enables synthesis and exploration of hitherto unknown functionalized nanographenes.
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