Photo-induced ruthenium-catalyzed alkene C–H-arylation at room temperature

C-H arylation has surfaced as a powerful tool for molecular sciences, with alkene C-H arylation thus far requiring either high reaction temperatures of 120 °C or stoichiometric amounts of RMgX. In sharp contrast, we herein report on room-temperature C-H arlyations of alkenes by means of ruthenium(II) catalysis with ample scope. This strategy also enabled late-stage diversification of structurally complex molecules and mechanistic studies provided strong evidence for photo-excitation of a ruthenacycle intermediate.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc04527d
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Photo-induced ruthenium-catalyzed alkene C–H-arylation at room temperature

Tanumoy Mandal, Lutz Ackermann, Sven Trienes, Stéphane Golling
Chemical Communications
Catalytic C–H Functionalization Methods
article

Photo-induced ruthenium-catalyzed alkene C–H-arylation at room temperature

Tanumoy Mandal, Lutz Ackermann, Sven Trienes, Stéphane Golling
article en

Abstract

C-H arylation has surfaced as a powerful tool for molecular sciences, with alkene C-H arylation thus far requiring either high reaction temperatures of 120 °C or stoichiometric amounts of RMgX. In sharp contrast, we herein report on room-temperature C-H arlyations of alkenes by means of ruthenium(II) catalysis with ample scope. This strategy also enabled late-stage diversification of structurally complex molecules and mechanistic studies provided strong evidence for photo-excitation of a ruthenacycle intermediate.

Chemical CommunicationsVol. 61(87)
German Centre for Cardiovascular Research (DE), University of Göttingen (DE)
Deutsches Zentrum für Herz-Kreislaufforschung, Deutscher Akademischer Austauschdienst, Deutsche Forschungsgemeinschaft, Gottfried Wilhelm Leibniz Universität Hannover, Leibniz-Gemeinschaft
Openalex Percentile: Top 80%
Catalytic C–H Functionalization Methods
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