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Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis

Herein we report a workflow coupling photoredox-nickel dual-catalyzed N-arylation reactions to benchtop analysis for the efficient generation of fragment-based libraries. Technological advances in photoreactor design facilitated reliable and reproducible experimentation. Knowledge on the reactivity...

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Detalles Bibliográficos
Autores principales: Lefebvre, Quentin, Salomé, Christophe, Fessard, Thomas C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237803/
https://www.ncbi.nlm.nih.gov/pubmed/32509029
http://dx.doi.org/10.3762/bjoc.16.87
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author Lefebvre, Quentin
Salomé, Christophe
Fessard, Thomas C
author_facet Lefebvre, Quentin
Salomé, Christophe
Fessard, Thomas C
author_sort Lefebvre, Quentin
collection PubMed
description Herein we report a workflow coupling photoredox-nickel dual-catalyzed N-arylation reactions to benchtop analysis for the efficient generation of fragment-based libraries. Technological advances in photoreactor design facilitated reliable and reproducible experimentation. Knowledge on the reactivity under previously reported reaction conditions of spirocyclic and strained heterocyclic building blocks, viewed as chemistry informers, could thus be rapidly accessed, identifying privileged or challenging scaffolds and paving the way for further exploration.
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spelling pubmed-72378032020-06-04 Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis Lefebvre, Quentin Salomé, Christophe Fessard, Thomas C Beilstein J Org Chem Full Research Paper Herein we report a workflow coupling photoredox-nickel dual-catalyzed N-arylation reactions to benchtop analysis for the efficient generation of fragment-based libraries. Technological advances in photoreactor design facilitated reliable and reproducible experimentation. Knowledge on the reactivity under previously reported reaction conditions of spirocyclic and strained heterocyclic building blocks, viewed as chemistry informers, could thus be rapidly accessed, identifying privileged or challenging scaffolds and paving the way for further exploration. Beilstein-Institut 2020-05-12 /pmc/articles/PMC7237803/ /pubmed/32509029 http://dx.doi.org/10.3762/bjoc.16.87 Text en Copyright © 2020, Lefebvre et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Lefebvre, Quentin
Salomé, Christophe
Fessard, Thomas C
Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title_full Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title_fullStr Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title_full_unstemmed Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title_short Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
title_sort accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237803/
https://www.ncbi.nlm.nih.gov/pubmed/32509029
http://dx.doi.org/10.3762/bjoc.16.87
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