2019•New Journal of ChemistryOpen access

σ-Holes promote the concertedness in nucleophilic aromatic substitution reactions of nitroarenes

Sebastián Gallardo‐Fuentes, Rodrigo Ormazábal‐Toledo

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Abstract

Concertedness in SNAr may be modulated by the presence of a σ-hole.

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What this paper is about

Concertedness in SNAr may be modulated by the presence of a σ-hole.

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OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Concertedness in SNAr may be modulated by the presence of a σ-hole.

Key concepts: Chemistry, Nucleophilic aromatic substitution, Nucleophilic substitution, Substitution reaction, Radical-nucleophilic aromatic substitution, Nucleophile, Substitution (logic), Medicinal chemistry

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σ-Holes promote the concertedness in nucleophilic aromatic substitution reactions of nitroarenes — Research Paper | ScholarLens

σ-Holes promote the concertedness in nucleophilic aromatic substitution reactions of nitroarenes

About this research paper

What this paper is about

Why it matters

Key contribution

Method / approach

Main findings

Limitations

Applications

Available abstract

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