One-Pot Synthesis of Bicyclo[2.2.1]heptane Derivatives by Three-Component Coupling of Norbornene, Aryl Halides, and Arylacetylenes in the Presence of Ligand-Free Palladium Catalytic Systems

The results of palladium-catalyzed difunctionalization of norbornene via one-pot three-component coupling with aryl halides and arylacetylenes with the formation of new Csp3–Csp2/Csp3–Csp bonds are reported. The proposed method is advantageous in comparison to other methods due to the use of a simple ligand-free catalytic system based on palladium salts and inorganic base for the preparation of valuable bicyclo[2.2.1]­heptane derivatives.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1134/s1070428025601050
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

One-Pot Synthesis of Bicyclo[2.2.1]heptane Derivatives by Three-Component Coupling of Norbornene, Aryl Halides, and Arylacetylenes in the Presence of Ligand-Free Palladium Catalytic Systems

Н. А. Лагода, А. F. Schmidt, Е. В. Ларина, А. А. Курохтина
Russian Journal of Organic Chemistry
Catalytic Cross-Coupling Reactions
article

One-Pot Synthesis of Bicyclo[2.2.1]heptane Derivatives by Three-Component Coupling of Norbornene, Aryl Halides, and Arylacetylenes in the Presence of Ligand-Free Palladium Catalytic Systems

Н. А. Лагода, А. F. Schmidt, Е. В. Ларина, А. А. Курохтина
article en

Abstract

The results of palladium-catalyzed difunctionalization of norbornene via one-pot three-component coupling with aryl halides and arylacetylenes with the formation of new Csp3–Csp2/Csp3–Csp bonds are reported. The proposed method is advantageous in comparison to other methods due to the use of a simple ligand-free catalytic system based on palladium salts and inorganic base for the preparation of valuable bicyclo[2.2.1]­heptane derivatives.

Russian Journal of Organic ChemistryVol. 61(4)
Irkutsk State University (RU)
Openalex Percentile: Top 90%
Catalytic Cross-Coupling Reactions
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