ReviewMolecules (Basel, Switzerland)2021
Synthetic Applications of Aziridinium Ions.
Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 24 citations in OpenAlex.
- Direct Aziridine Synthesis from Amines and Styrene Derivatives via a Base-Promoted Oxidative Cascade Reaction.Journal of the American Chemical Society · 2026Article
- Unlocking the C-centered ring-opening of phosphiranium ions for a straightforward entry to functionalized phosphines.Nature communications · 2024Article
- Article
- Regioselective ring opening of aziridine for synthesizing azaheterocycle.Frontiers in chemistry · 2023Article
- Atom Economical Multi-Substituted Pyrrole Synthesis from Aziridine.Molecules (Basel, Switzerland) · 2022Article
- Tunable Aziridinium Ylide Reactivity: Non-covalent Interactions Enable Divergent Product Outcomes.ACS catalysis · 2022Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nonactivated aziridine with an electron-donating group at the ring nitrogen should be activated to an aziridinium ion prior to being converted to cyclic and acyclic nitrogen-containing molecules. This review describes ways to generate aziridinium ions and their utilization for synthetic purposes. Specifically, the intra- and intermolecular formation of aziridinium ions with proper electrophiles are classified, and their regio- and stereoselective transformations with nucleophiles are described on the basis of recent developments.
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Registered trials
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