Suzuki-Miyaura coupling of aryl iodides, bromides, and chlorides catalyzed by bis(thiazole) pincer palladium complexes.

@article{Luo2012SuzukiMiyauraCO,
  title={Suzuki-Miyaura coupling of aryl iodides, bromides, and chlorides catalyzed by bis(thiazole) pincer palladium complexes.},
  author={Qun-Li Luo and Jian-Ping Tan and Zhi-Fu Li and Wen-Hui Nan and Dong-Rong Xiao},
  journal={The Journal of organic chemistry},
  year={2012},
  volume={77 18},
  pages={8332-7}
}
Bis(thiazole) pincer palladium complexes showed efficient catalytic activity for the Suzuki-Miyaura coupling of aryl halides, allowing the synthesis of biaryls with very high turnover numbers and turnover frequencies. The complexes were successfully applied in the scalable and green synthesis of the key intermediates of bioactive LUF5771 and its analogues. 

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