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N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis

We show that N,N-dimethylformamide-stabilized Pd nanoclusters (NCs) have high catalytic activity in the reaction of substituted 2-iodoanilines with alkynes to give 2,3-disubstituted indoles. This indole synthesis does not require phosphine ligands and proceeds with low Pd catalyst loadings. The Pd N...

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Detalles Bibliográficos
Autores principales: Onishi, Kaito, Oikawa, Kei, Yano, Hiroki, Suzuki, Takeyuki, Obora, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079145/
https://www.ncbi.nlm.nih.gov/pubmed/35542799
http://dx.doi.org/10.1039/c8ra01410h
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author Onishi, Kaito
Oikawa, Kei
Yano, Hiroki
Suzuki, Takeyuki
Obora, Yasushi
author_facet Onishi, Kaito
Oikawa, Kei
Yano, Hiroki
Suzuki, Takeyuki
Obora, Yasushi
author_sort Onishi, Kaito
collection PubMed
description We show that N,N-dimethylformamide-stabilized Pd nanoclusters (NCs) have high catalytic activity in the reaction of substituted 2-iodoanilines with alkynes to give 2,3-disubstituted indoles. This indole synthesis does not require phosphine ligands and proceeds with low Pd catalyst loadings. The Pd NCs were separated from the mixture after the reaction, and recycled at least three times. Transmission electron microscopy images showed that the Pd particle size before the reaction was 1.5–2.5 nm. The particle size after the reaction was 2–3 nm. X-ray photoelectron spectroscopy showed that the binding energy of the Pd NCs before the reaction was 335.0 eV.
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spelling pubmed-90791452022-05-09 N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis Onishi, Kaito Oikawa, Kei Yano, Hiroki Suzuki, Takeyuki Obora, Yasushi RSC Adv Chemistry We show that N,N-dimethylformamide-stabilized Pd nanoclusters (NCs) have high catalytic activity in the reaction of substituted 2-iodoanilines with alkynes to give 2,3-disubstituted indoles. This indole synthesis does not require phosphine ligands and proceeds with low Pd catalyst loadings. The Pd NCs were separated from the mixture after the reaction, and recycled at least three times. Transmission electron microscopy images showed that the Pd particle size before the reaction was 1.5–2.5 nm. The particle size after the reaction was 2–3 nm. X-ray photoelectron spectroscopy showed that the binding energy of the Pd NCs before the reaction was 335.0 eV. The Royal Society of Chemistry 2018-03-22 /pmc/articles/PMC9079145/ /pubmed/35542799 http://dx.doi.org/10.1039/c8ra01410h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Onishi, Kaito
Oikawa, Kei
Yano, Hiroki
Suzuki, Takeyuki
Obora, Yasushi
N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title_full N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title_fullStr N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title_full_unstemmed N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title_short N,N-Dimethylformamide-stabilized palladium nanoclusters as a catalyst for Larock indole synthesis
title_sort n,n-dimethylformamide-stabilized palladium nanoclusters as a catalyst for larock indole synthesis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079145/
https://www.ncbi.nlm.nih.gov/pubmed/35542799
http://dx.doi.org/10.1039/c8ra01410h
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