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Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism

Palladium catalysis induced by visible-light irradiation is a promising tool for promoting unusual chemical transformations. We describe the development of excited-state palladium-catalyzed reductive alkylation of imines with alkyl bromides. The new methodology shows broad functional group tolerance...

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Autores principales: Kancherla, Rajesh, Muralirajan, Krishnamoorthy, Rueping, Magnus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337745/
https://www.ncbi.nlm.nih.gov/pubmed/35974758
http://dx.doi.org/10.1039/d2sc02363f
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author Kancherla, Rajesh
Muralirajan, Krishnamoorthy
Rueping, Magnus
author_facet Kancherla, Rajesh
Muralirajan, Krishnamoorthy
Rueping, Magnus
author_sort Kancherla, Rajesh
collection PubMed
description Palladium catalysis induced by visible-light irradiation is a promising tool for promoting unusual chemical transformations. We describe the development of excited-state palladium-catalyzed reductive alkylation of imines with alkyl bromides. The new methodology shows broad functional group tolerance and can additionally be applied in the direct three-component reaction of aldehydes, anilines, and alkyl bromides to give the alkyl amines under mild reaction conditions. Time-resolved photoluminescence experiments allowed the determination of the excited-state reaction kinetics and indicate that the reaction is proceeding via the inner-sphere electron transfer mechanism.
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spelling pubmed-93377452022-08-15 Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism Kancherla, Rajesh Muralirajan, Krishnamoorthy Rueping, Magnus Chem Sci Chemistry Palladium catalysis induced by visible-light irradiation is a promising tool for promoting unusual chemical transformations. We describe the development of excited-state palladium-catalyzed reductive alkylation of imines with alkyl bromides. The new methodology shows broad functional group tolerance and can additionally be applied in the direct three-component reaction of aldehydes, anilines, and alkyl bromides to give the alkyl amines under mild reaction conditions. Time-resolved photoluminescence experiments allowed the determination of the excited-state reaction kinetics and indicate that the reaction is proceeding via the inner-sphere electron transfer mechanism. The Royal Society of Chemistry 2022-07-07 /pmc/articles/PMC9337745/ /pubmed/35974758 http://dx.doi.org/10.1039/d2sc02363f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kancherla, Rajesh
Muralirajan, Krishnamoorthy
Rueping, Magnus
Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title_full Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title_fullStr Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title_full_unstemmed Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title_short Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
title_sort excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337745/
https://www.ncbi.nlm.nih.gov/pubmed/35974758
http://dx.doi.org/10.1039/d2sc02363f
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