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Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis

Catalytic asymmetric dearomatization of heteroaromatic compounds has received considerable attention in the last few years, since it allows for a fast expansion of the chemical space by converting relatively simple, flat molecules into complex, three dimensional structures with added value. Among di...

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Detalles Bibliográficos
Autores principales: Aleksiev, Martin, García Mancheño, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019134/
https://www.ncbi.nlm.nih.gov/pubmed/36790499
http://dx.doi.org/10.1039/d2cc07101k
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author Aleksiev, Martin
García Mancheño, Olga
author_facet Aleksiev, Martin
García Mancheño, Olga
author_sort Aleksiev, Martin
collection PubMed
description Catalytic asymmetric dearomatization of heteroaromatic compounds has received considerable attention in the last few years, since it allows for a fast expansion of the chemical space by converting relatively simple, flat molecules into complex, three dimensional structures with added value. Among different approaches, remarkable progress has been recently achieved by the development of organocatalytic dearomatization methods. In particular, the anion-binding catalysis technology has emerged as a potent alternative to metal catalysis, which together with the design of novel, tunable anion-receptor motifs, has provided new entries for the enantioselective dearomatization of heteroarenes through a chiral contact ion pair formation by activation of the electrophilic reaction partner. In this feature, we provide an overview of the different methodologies and advances in anion-binding catalyzed dearomatization reactions of different heteroarenes.
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spelling pubmed-100191342023-03-17 Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis Aleksiev, Martin García Mancheño, Olga Chem Commun (Camb) Chemistry Catalytic asymmetric dearomatization of heteroaromatic compounds has received considerable attention in the last few years, since it allows for a fast expansion of the chemical space by converting relatively simple, flat molecules into complex, three dimensional structures with added value. Among different approaches, remarkable progress has been recently achieved by the development of organocatalytic dearomatization methods. In particular, the anion-binding catalysis technology has emerged as a potent alternative to metal catalysis, which together with the design of novel, tunable anion-receptor motifs, has provided new entries for the enantioselective dearomatization of heteroarenes through a chiral contact ion pair formation by activation of the electrophilic reaction partner. In this feature, we provide an overview of the different methodologies and advances in anion-binding catalyzed dearomatization reactions of different heteroarenes. The Royal Society of Chemistry 2023-02-15 /pmc/articles/PMC10019134/ /pubmed/36790499 http://dx.doi.org/10.1039/d2cc07101k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Aleksiev, Martin
García Mancheño, Olga
Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title_full Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title_fullStr Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title_full_unstemmed Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title_short Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
title_sort enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019134/
https://www.ncbi.nlm.nih.gov/pubmed/36790499
http://dx.doi.org/10.1039/d2cc07101k
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