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Organogelation enables fast organolithium cross-coupling reactions in air

C–C bond formation based on palladium-catalysed cross-coupling reactions using organolithium reagents has seen major breakthroughs in the past decade. However, the use of inert conditions, as well as slow addition of the organolithium species, is generally required. Here we describe the Pd-catalysed...

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Detalles Bibliográficos
Autores principales: Visser, Paco, Feringa, Ben L.
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/PMC10157804/
https://www.ncbi.nlm.nih.gov/pubmed/37074292
http://dx.doi.org/10.1039/d3cc00756a
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author Visser, Paco
Feringa, Ben L.
author_facet Visser, Paco
Feringa, Ben L.
author_sort Visser, Paco
collection PubMed
description C–C bond formation based on palladium-catalysed cross-coupling reactions using organolithium reagents has seen major breakthroughs in the past decade. However, the use of inert conditions, as well as slow addition of the organolithium species, is generally required. Here we describe the Pd-catalysed cross-coupling of C(36)H(74)-gelated organolithium reagents with aryl bromides. The reaction proceeds in 5 min at room temperature, while eliminating the previously required slow addition, and strict use of inert atmosphere. Crucially, the use of organolithium gels facilitates handling, and offers a tremendously increased process safety, which is illustrated by a gram-scale transformation that does not require any extraordinary safety precautions.
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spelling pubmed-101578042023-05-05 Organogelation enables fast organolithium cross-coupling reactions in air Visser, Paco Feringa, Ben L. Chem Commun (Camb) Chemistry C–C bond formation based on palladium-catalysed cross-coupling reactions using organolithium reagents has seen major breakthroughs in the past decade. However, the use of inert conditions, as well as slow addition of the organolithium species, is generally required. Here we describe the Pd-catalysed cross-coupling of C(36)H(74)-gelated organolithium reagents with aryl bromides. The reaction proceeds in 5 min at room temperature, while eliminating the previously required slow addition, and strict use of inert atmosphere. Crucially, the use of organolithium gels facilitates handling, and offers a tremendously increased process safety, which is illustrated by a gram-scale transformation that does not require any extraordinary safety precautions. The Royal Society of Chemistry 2023-04-17 /pmc/articles/PMC10157804/ /pubmed/37074292 http://dx.doi.org/10.1039/d3cc00756a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Visser, Paco
Feringa, Ben L.
Organogelation enables fast organolithium cross-coupling reactions in air
title Organogelation enables fast organolithium cross-coupling reactions in air
title_full Organogelation enables fast organolithium cross-coupling reactions in air
title_fullStr Organogelation enables fast organolithium cross-coupling reactions in air
title_full_unstemmed Organogelation enables fast organolithium cross-coupling reactions in air
title_short Organogelation enables fast organolithium cross-coupling reactions in air
title_sort organogelation enables fast organolithium cross-coupling reactions in air
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157804/
https://www.ncbi.nlm.nih.gov/pubmed/37074292
http://dx.doi.org/10.1039/d3cc00756a
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