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Citation: LI Tian, MA Kai-Guo, GAO Zhen, LI Wei-Hong. A Brief Introduction to Suzuki-Miyaura Coupling Reaction in Organic Lab Abroad[J]. University Chemistry, ;2016, 31(10): 98-104. doi: 10.3866/PKU.DXHX201602011 shu

A Brief Introduction to Suzuki-Miyaura Coupling Reaction in Organic Lab Abroad

Experimental Chemistry Center, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P. R. China

Suzuki-Miyaura reaction is a coupling process of aryl boric acid (boron ester) and aryl halide that catalyzed by palladium (0).The reaction shows well tolerance for various functional groups and is wildly applied in syntheses of natural products and organic materials.Recently,colleges abroad tried to introduce this reaction into the undergraduate organic lab.This paper collected the literatures in Journal of Chemical Education about the Suzuki-Miyaura reaction since 2000 and gave an overview.
- Suzuki-Miyaura coupling reaction,
- Experimental design
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  Wen WANG , Ying XU , Gang XIONG , Lixin YOU , Yaguang SUN . Pd-NHC-functionalized La-metal-organic framework for efficient Suzuki-Miyaura cross-coupling reaction. Chinese Journal of Inorganic Chemistry, 2026, 42(7): 1475-1484. doi: 10.11862/CJIC.20260025
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