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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9337745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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