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Charge Delocalization and Enhanced Acidity in Tricationic Superelectrophiles

https://doi.org/10.1021/ja2046364

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications

inferredcites →https://doi.org/10.1002/anie.198303901openalex-snapshot

Stable Carbodications

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Selective electrophilic activation of alkanes

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Electrophilic reactions at single bonds. XVIII. Indication of protosolvated de facto substituting agents in the reactions of alkanes with acetylium and nitronium ions in superacidic media

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Prediction of substituent sensitivities (.rho.R+) for carbocations. Correlation with charges or HOMO-LUMO interactions

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13C NMR/DFT/GIAO Studies of Phenylene Bis(1,3-dioxolanium) Dications and 2,4,6-Triphenylene Tris(1,3-dioxolanium) Trication

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1016/j.mencom.2015.01.003openalex-snapshot

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