Topic
Radical-nucleophilic aromatic substitution
About: Radical-nucleophilic aromatic substitution is a research topic. Over the lifetime, 1563 publications have been published within this topic receiving 36220 citations.
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01 Jun 1977
TL;DR: Localized Chemical bonding Delocalized Chemical Bonding Bonding Weaker than Covalent Stereochemistry Carbocations, Carbanions, Free Radicals, Carbenes and Nitrenes Mechanisms and Methods of Determining them Photochemistry Acids and Bases Effects of Structure on Reactivity Aliphatic Nucleophilic Substitution Aromatic Electrophilic Substitutes Aliphatically Electrophilic Substitution Free-Radical Substitution Addition to Carbon-Carbon Multiple Bonds Adding to Carbon Hetero Multiple Bonds Eliminations Rearrangements Ox
Abstract: Localized Chemical bonding Delocalized Chemical Bonding Bonding Weaker than Covalent Stereochemistry Carbocations, Carbanions, Free Radicals, Carbenes and Nitrenes Mechanisms and Methods of Determining Them Photochemistry Acids and Bases Effects of Structure on Reactivity Aliphatic Nucleophilic Substitution Aromatic Electrophilic Substitution Aliphatic Electrophilic Substitution Free-Radical Substitution Addition to Carbon-Carbon Multiple Bonds Addition to Carbon- Hetero Multiple Bonds Eliminations Rearrangements Oxidations and Reductions The Literature of Organic Chemistry Classifications of Reactions by Type of Compound Synthesized.
4,885 citations
1,046 citations
796 citations
TL;DR: A simple analogy between acid/base catalysis and redox catalysis is presented, and the 'electron is a catalyst' paradigm unifies mechanistically an assortment of synthetic transformations that otherwise have little or no apparent relationship.
Abstract: This Review draws an analogy between acid–base catalysis and redox catalysis. The 'electron is a catalyst' paradigm unifies mechanistically an assortment of synthetic transformations that otherwise have little or no apparent relationship. Various radical cascades catalysed by the electron are discussed.
510 citations
468 citations