Mechanochemical Sequential Deoxygenative Cross-Coupling Reactions of Phenols Under Ruthenium-Nickel Catalysis

Herein, we report the first mechanochemical strategy for the Ru-catalyzed deoxygenative borylation of free phenols via C-O bond cleavage. This Ru-catalyzed phenolic borylation approach has been successfully extended to the Suzuki-Miyaura-type cross-coupling of phenols with aryl bromides. The protocol accepts a wide scope of phenolic substrates, allowing the synthesis of aryl pinacolboranes and biphenyl structures in excellent yields and serving as a better alternative to classical cross-coupling reactions in the context of pot, atom, and step economy synthesis.

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Publication Details

Journal
Molecules
Published
2025-04-19
DOI
https://doi.org/10.3390/molecules30081835
Citations
4
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
3.74

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article

Mechanochemical Sequential Deoxygenative Cross-Coupling Reactions of Phenols Under Ruthenium-Nickel Catalysis

Vitaliy Yepishev, Sehrish Sarfaraz, Ronak V. Prajapati, Viktor O. Iaroshenko et al.
4 citations
Molecules
Catalytic Cross-Coupling Reactions
3.74
article

Mechanochemical Sequential Deoxygenative Cross-Coupling Reactions of Phenols Under Ruthenium-Nickel Catalysis

Vitaliy Yepishev, Sehrish Sarfaraz, Ronak V. Prajapati, Viktor O. Iaroshenko, Khurshid Ayub, Yevhen Karpun, Vaibhav D. Prajapati, Satenik Mkrtchyan, Michał Jakubczyk, Gabriela Addová, Juraj Filo, Vishal B. Purohit, Michael G. Garcia, Manoj K. Saini
article en
4 citations

Abstract

Herein, we report the first mechanochemical strategy for the Ru-catalyzed deoxygenative borylation of free phenols via C-O bond cleavage. This Ru-catalyzed phenolic borylation approach has been successfully extended to the Suzuki-Miyaura-type cross-coupling of phenols with aryl bromides. The protocol accepts a wide scope of phenolic substrates, allowing the synthesis of aryl pinacolboranes and biphenyl structures in excellent yields and serving as a better alternative to classical cross-coupling reactions in the context of pot, atom, and step economy synthesis.

MoleculesVol. 30(8)
Osnabrück University (DE), Gulf University for Science & Technology (KW), Abbottabad University of Science and Technology (PK), Charotar University of Science and Technology (IN), Czech Academy of Sciences, Institute of Inorganic Chemistry (CZ), Georgian American University (GE), Sardar Patel University (IN), Matej Bel University (SK), Chitkara University (IN), Comenius University Bratislava (SK), Banaras Hindu University (IN)
Agentúra na Podporu Výskumu a Vývoja
Openalex Percentile: Top 8%
Catalytic Cross-Coupling Reactions
3.74
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