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The SRN1 reaction

Bardagi, Javier Ivan et al · John Wiley & Sons Ltd · 2012

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Since its discovery, the radical nucleophilic substitution, or SRN1 reaction, has been widely used to achieve new CC or C-heteroatom bonds. The mechanism involves a chain propagation cycle with radicals and radical anions as intermediates. The initiation step is an electron transfer to a substrate to form its radical anion, which fragments to afford a radical and the anion of the leaving group. The radical thus formed couples with a nucleophile to give a new radical anion which, in the next propagation step, transfers its extra electron to the substrate, closing the cycle. Here we discuss SRN1 reactions of aromatic substrates with carbanions and heteroaromatic nucleophiles as well as ring-closure reactions to obtain heterocycles by different approaches. SRN1 reactions of vinylic halides with nucleophiles and the competing mechanisms are also examined. Reactions of aliphatic substrates that do not react or are poorly reactive toward polar nucleophilic substitutions (cycloalkyl, bridgehead, neopentyl, and perfluoroalkyl halides) are discussed in terms of mechanistic requirements to follow an SRN1 process. In addition, the reactions of alkyl substrates with electron-withdrawing groups also are presented. Every year, new synthetic strategies and mechanistic studies involving SRN1 reactions are reported, which constitute a useful tool in the field of organic chemistry. Fil: Bardagi, Javier Ivan. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Vaillard, Victoria Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina

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APA 7

Bardagi, J. I. E. A. (2012). The SRN1 reaction. John Wiley & Sons Ltd. http://hdl.handle.net/11336/245996

MLA

Bardagi, Javier Ivan et al. The SRN1 reaction. John Wiley & Sons Ltd, 2012. http://hdl.handle.net/11336/245996.

Chicago

Bardagi, Javier Ivan et al. 2012. The SRN1 reaction. John Wiley & Sons Ltd. http://hdl.handle.net/11336/245996.

Harvard

Bardagi, J. I. E. A. 2012, The SRN1 reaction, John Wiley & Sons Ltd, available at: http://hdl.handle.net/11336/245996 [Accessed 10 Aug. 2026].

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Title
The SRN1 reaction
Author / contributors
Bardagi, Javier Ivan et al
Publisher
John Wiley & Sons Ltd
Publication year
2012
Language
English

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