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Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction

[Image: see text] Herein, we discuss the formation and reactivity of 1-imidocarbenium cations in Friedel–Crafts-type reaction between 1-imidoalkylphosphonium salts and arenes. The observed weakening of C(α)–P(+) bond is described qualitatively and quantitatively. The determination of rate constants...

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Autores principales: Adamek, Jakub, Mazurkiewicz, Roman, Węgrzyk-Schlieter, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434785/
https://www.ncbi.nlm.nih.gov/pubmed/36061720
http://dx.doi.org/10.1021/acsomega.2c03930
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author Adamek, Jakub
Mazurkiewicz, Roman
Węgrzyk-Schlieter, Anna
author_facet Adamek, Jakub
Mazurkiewicz, Roman
Węgrzyk-Schlieter, Anna
author_sort Adamek, Jakub
collection PubMed
description [Image: see text] Herein, we discuss the formation and reactivity of 1-imidocarbenium cations in Friedel–Crafts-type reaction between 1-imidoalkylphosphonium salts and arenes. The observed weakening of C(α)–P(+) bond is described qualitatively and quantitatively. The determination of rate constants and activation energies of C(α)–P(+) bond cleavage enabled systematic reactivity investigations of a series of phosphonium salts with different structures. Finally, the application scope for the imidoalkylation of aromatic hydrocarbons was explored. The results confirm that the generated 1-imidocarbenium cations are reactive enough to alkylate strongly activated, less-activated, or even inactivated aromatic compounds.
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spelling pubmed-94347852022-09-02 Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction Adamek, Jakub Mazurkiewicz, Roman Węgrzyk-Schlieter, Anna ACS Omega [Image: see text] Herein, we discuss the formation and reactivity of 1-imidocarbenium cations in Friedel–Crafts-type reaction between 1-imidoalkylphosphonium salts and arenes. The observed weakening of C(α)–P(+) bond is described qualitatively and quantitatively. The determination of rate constants and activation energies of C(α)–P(+) bond cleavage enabled systematic reactivity investigations of a series of phosphonium salts with different structures. Finally, the application scope for the imidoalkylation of aromatic hydrocarbons was explored. The results confirm that the generated 1-imidocarbenium cations are reactive enough to alkylate strongly activated, less-activated, or even inactivated aromatic compounds. American Chemical Society 2022-08-15 /pmc/articles/PMC9434785/ /pubmed/36061720 http://dx.doi.org/10.1021/acsomega.2c03930 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Adamek, Jakub
Mazurkiewicz, Roman
Węgrzyk-Schlieter, Anna
Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title_full Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title_fullStr Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title_full_unstemmed Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title_short Generation and Reactivity of 1-Imidocarbenium Cations in the Friedel–Crafts-type Reaction
title_sort generation and reactivity of 1-imidocarbenium cations in the friedel–crafts-type reaction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434785/
https://www.ncbi.nlm.nih.gov/pubmed/36061720
http://dx.doi.org/10.1021/acsomega.2c03930
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