Palladium-Catalyzed Deoxygenative Deuteration of Aryl Nonaflates

The palladium-catalyzed synthesis of deuterated aromatics through deoxygenative deuteration of aryl nonaflates has been achieved in good to high yields with high D contents. In this process, a variety of functional groups and heterocyclic moieties were well tolerated, and the double incorporation of deuterium also proceeded smoothly. As well as the synthesis of a deuterated estrone derivative, the gram-scale experiment was conducted with sufficient efficiency, showing the promising potentiality of this method.

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Publication Details

Journal
Synthesis
Published
2026-10-28
DOI
https://doi.org/10.1055/a-2991-3391
Primary Topic
Chemical Reactions and Isotopes
Type
article
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article

Palladium-Catalyzed Deoxygenative Deuteration of Aryl Nonaflates

Yosuke Demizu, Osamu Onomura, Kotaro Tsukuda, Masami Kuriyama et al.
1 links
Synthesis
Chemical Reactions and Isotopes
article

Palladium-Catalyzed Deoxygenative Deuteration of Aryl Nonaflates

Yosuke Demizu, Osamu Onomura, Kotaro Tsukuda, Masami Kuriyama, Kosuke Yamamoto, Kazuya Kamata, Reo Wakiyama, Tetsuro Morimoto
article en

Abstract

The palladium-catalyzed synthesis of deuterated aromatics through deoxygenative deuteration of aryl nonaflates has been achieved in good to high yields with high D contents. In this process, a variety of functional groups and heterocyclic moieties were well tolerated, and the double incorporation of deuterium also proceeded smoothly. As well as the synthesis of a deuterated estrone derivative, the gram-scale experiment was conducted with sufficient efficiency, showing the promising potentiality of this method.

Synthesis
University of Nagasaki (JP), National Institute of Health Sciences (JP), Nagasaki University (JP)
Openalex Percentile: Top 15%
Chemical Reactions and Isotopes
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