Intrinsic relative nucleophilicity of indoles

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作者
Eduardo Chamorro
Mario Duque-Noreña
Mar Ríos-Gutiérrez
Luis R. Domingo
Patricia Pérez
机构
[1] Universidad Andres Bello,Departamento de Ciencias Químicas, Millennium Nucleus Chemical Processes and Catalysis (CPC), Facultad de Ciencias Exactas
[2] Universidad de Valencia,Departamento de Química Orgánica
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Nucleophilicity; Electrophilicity; Conceptual DFT; Indoles; Reactivity Scales; Polar organic reactions;
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摘要
The range of applicability of intrinsic (i.e., electronic) relative indices for quantifying electrophilicity and nucleophilicity responses (Chamorro et al. in J Phys Chem A 117(12):2636–2643, 2013) is extended to the characterization of coupling reactions of indoles with benzhydrylium ions and with the strongly electron-deficient heteroarene 4,6-dinitrobenzofuroxan. The reactivity categorization based on experimental kinetic evidence for such a electrophile/nucleophile coupling (Lakhdar et al. in J Org Chem 71(24):9088–9095, 2006) is rationalized in terms of purely electronic descriptors, revealing the polar nucleophilic activation of indole as a key factor associated with the initial rate-determining C–C coupling process.
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