浅谈国外“Suzuki-Miyaura金属偶联反应”的教学设计思路

doi:10.3866/PKU.DXHX201602011

Abstract

Abstract:

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.

Key words: Suzuki-Miyaura coupling reaction, Experimental design

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

References

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

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