Chinese Journal of Organic Chemistry >
Recent Advance of Transition Metal-Free Catalyzed Suzuki-Type Cross Coupling Reaction
Received date: 2022-08-06
Revised date: 2022-09-25
Online published: 2022-11-01
Supported by
Fundamental Research Funds for the Central Universities(2572020BU03); China Postdoctoral Science Foundation Funded Project(2020M681065); Heilongjiang Postdoctoral Fund(LBH-Z20103)
Transition metal catalyzed Suzuki coupling reaction serves as one of the most versatile and widespread methods for the C-C bonds formation, which greatly promotes the development of synthetic chemistry. Currently, the Suzuki coupling reactions heavily rely on noble palladium-catalyzed system. However, the high cost, toxicity and low reserves of palladium have become the main obstacles for their development in organic synthesis. Over the past two decades, metal-free catalyzed Suzuki-Type cross coupling reactions earned extensive concern, and a large number of efficient and new reaction systems have been reported. In this review, the recent progresses of metal-free catalyzed Suzuki-Type cross coupling reactions are summarized, mainly including bases, organometallic reagents and organic molecules promoted reactions. In addition, the mechanism of reaction is also discussed in this review.
Biao Ma , Miaomiao Zhang , Zhanyu Li , Jinsong Peng , Chunxia Chen . Recent Advance of Transition Metal-Free Catalyzed Suzuki-Type Cross Coupling Reaction[J]. Chinese Journal of Organic Chemistry, 2023 , 43(2) : 455 -470 . DOI: 10.6023/cjoc202208008
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