Synthesis of Biheteroaryls by Pd-Catalyzed Homocoupling of Heteroaryl Bromides

Symmetrical biheteroaryl compounds, such as bypyridines and bipyrazoles, are important ligands in transition-metal catalysis. They also serve as synthetic precursors of photo catalysts/sensitizers, bioactive agents, and energetic materials. To facilitate the concise synthesis of these useful structures, an efficient Pd-catalyzed homocoupling of heteroaryl bromides has been successfully established using the electron-rich and sterically hindered monophosphorus ligand BIDIME. The coupling protocol features a tandem Miyaura borylation/Suzuki coupling sequence and exhibits unprecedented tolerance of a wide range of heteroaryl bromides, providing a series of symmetrical biheteroaryls in moderate to good yields. Notably, the use of the corresponding polymeric ligand, PolyBIDIME, enabled the recycling of a palladium catalyst, demonstrating the potential of the homocoupling in practical applications.

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Publication Details

Journal
Organic Letters
Published
2024-10-07
DOI
https://doi.org/10.1021/acs.orglett.4c03060
Citations
6
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.50

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article

Synthesis of Biheteroaryls by Pd-Catalyzed Homocoupling of Heteroaryl Bromides

Wenjun Tang, He Yang, Bangke Luo, Qianjiao Ma et al.
6 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.50
article

Synthesis of Biheteroaryls by Pd-Catalyzed Homocoupling of Heteroaryl Bromides

Wenjun Tang, He Yang, Bangke Luo, Qianjiao Ma, Wenfeng Dong
article en
6 citations

Abstract

Symmetrical biheteroaryl compounds, such as bypyridines and bipyrazoles, are important ligands in transition-metal catalysis. They also serve as synthetic precursors of photo catalysts/sensitizers, bioactive agents, and energetic materials. To facilitate the concise synthesis of these useful structures, an efficient Pd-catalyzed homocoupling of heteroaryl bromides has been successfully established using the electron-rich and sterically hindered monophosphorus ligand BIDIME. The coupling protocol features a tandem Miyaura borylation/Suzuki coupling sequence and exhibits unprecedented tolerance of a wide range of heteroaryl bromides, providing a series of symmetrical biheteroaryls in moderate to good yields. Notably, the use of the corresponding polymeric ligand, PolyBIDIME, enabled the recycling of a palladium catalyst, demonstrating the potential of the homocoupling in practical applications.

Organic LettersVol. 26(41)
Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, National Key Research and Development Program of China, Special Project for Research and Development in Key areas of Guangdong Province
Openalex Percentile: Top 19%
Catalytic C–H Functionalization Methods
1.50
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Synthesis of Biheteroaryls by Pd-Catalyzed Homocoupling of Heteroaryl Bromides — Wenjun Tang, He Yang, et al. · Organic Letters (2024) | TGRS Research Map | TGRS