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Strategies That Utilize Ion Pairing Interactions to Exert Selectivity Control in the Functionalization of C–H Bonds
[Image: see text] Electrostatic attraction between two groups of opposite charge, typically known as ion-pairing, offers unique opportunities for the design of systems to enable selectivity control in chemical reactions. Catalysis using noncovalent interactions is an established and vibrant research...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562467/ https://www.ncbi.nlm.nih.gov/pubmed/36178308 http://dx.doi.org/10.1021/jacs.2c08752 |
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author | Gillespie, James E. Fanourakis, Alexander Phipps, Robert J. |
author_facet | Gillespie, James E. Fanourakis, Alexander Phipps, Robert J. |
author_sort | Gillespie, James E. |
collection | PubMed |
description | [Image: see text] Electrostatic attraction between two groups of opposite charge, typically known as ion-pairing, offers unique opportunities for the design of systems to enable selectivity control in chemical reactions. Catalysis using noncovalent interactions is an established and vibrant research area, but it is noticeable that hydrogen bonding interactions are still the main interaction of choice in system design. Opposite charges experience the powerful force of Coulombic attraction and have the ability to exert fundamental influence on the outcome of reactions that involve charged reagents, intermediates or catalysts. In this Perspective, we will examine how ion-pairing interactions have been used to control selectivity in C–H bond functionalization processes. This broad class of reactions provides an interesting and thought-provoking lens through which to examine the application of ion-pairing design strategies because it is one that encompasses great mechanistic diversity, poses significant selectivity challenges, and perhaps most importantly is of immense interest to synthetic chemists in both industry and academia. We survey reactions that proceed via radical and ionic mechanisms alongside those that involve transition metal catalysis and will deal with control of site-selectivity and enantioselectivity. We anticipate that as this emerging area develops, it will become an ever-more important design strategy for selectivity control. |
format | Online Article Text |
id | pubmed-9562467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95624672022-10-15 Strategies That Utilize Ion Pairing Interactions to Exert Selectivity Control in the Functionalization of C–H Bonds Gillespie, James E. Fanourakis, Alexander Phipps, Robert J. J Am Chem Soc [Image: see text] Electrostatic attraction between two groups of opposite charge, typically known as ion-pairing, offers unique opportunities for the design of systems to enable selectivity control in chemical reactions. Catalysis using noncovalent interactions is an established and vibrant research area, but it is noticeable that hydrogen bonding interactions are still the main interaction of choice in system design. Opposite charges experience the powerful force of Coulombic attraction and have the ability to exert fundamental influence on the outcome of reactions that involve charged reagents, intermediates or catalysts. In this Perspective, we will examine how ion-pairing interactions have been used to control selectivity in C–H bond functionalization processes. This broad class of reactions provides an interesting and thought-provoking lens through which to examine the application of ion-pairing design strategies because it is one that encompasses great mechanistic diversity, poses significant selectivity challenges, and perhaps most importantly is of immense interest to synthetic chemists in both industry and academia. We survey reactions that proceed via radical and ionic mechanisms alongside those that involve transition metal catalysis and will deal with control of site-selectivity and enantioselectivity. We anticipate that as this emerging area develops, it will become an ever-more important design strategy for selectivity control. American Chemical Society 2022-09-30 2022-10-12 /pmc/articles/PMC9562467/ /pubmed/36178308 http://dx.doi.org/10.1021/jacs.2c08752 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 | Gillespie, James E. Fanourakis, Alexander Phipps, Robert J. Strategies That Utilize Ion Pairing Interactions to Exert Selectivity Control in the Functionalization of C–H Bonds |
title | Strategies That Utilize
Ion Pairing Interactions to
Exert Selectivity Control in the Functionalization of C–H Bonds |
title_full | Strategies That Utilize
Ion Pairing Interactions to
Exert Selectivity Control in the Functionalization of C–H Bonds |
title_fullStr | Strategies That Utilize
Ion Pairing Interactions to
Exert Selectivity Control in the Functionalization of C–H Bonds |
title_full_unstemmed | Strategies That Utilize
Ion Pairing Interactions to
Exert Selectivity Control in the Functionalization of C–H Bonds |
title_short | Strategies That Utilize
Ion Pairing Interactions to
Exert Selectivity Control in the Functionalization of C–H Bonds |
title_sort | strategies that utilize
ion pairing interactions to
exert selectivity control in the functionalization of c–h bonds |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562467/ https://www.ncbi.nlm.nih.gov/pubmed/36178308 http://dx.doi.org/10.1021/jacs.2c08752 |
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