4.8 Article

Direct Arylation of Imidazo[1,2-a]pyridine at C-3 with Aryl Iodides, Bromides, and Triflates via Copper(I)-Catalyzed C-H Bond Functionalization

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ORGANIC LETTERS
卷 14, 期 7, 页码 1688-1691

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol300232a

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资金

  1. Foundation for Distinguished Young Talentsin Higher Education of Guangdong, China [LYM11083]
  2. National Natural Science Foundation of China [20932002, 21172076]
  3. National Basic Research Program of China (973 Program) [2011CB808600]
  4. Ministry of Education of China [20090172110014]
  5. Guangdong Natural Science Foundation [10351064101000000]

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A convenient method for the copper(I)-catalyzed arylation of substituted imidazo[1,2-a]pyridine has been developed. This method is applicable to a variety of aryl electrophiles, including bromides, iodides, and triflates. It represents the first general process for C-3 arylation of substituted imidazo[1,2-a]pyridine by Cu(I) catalysis to construct various functionalized imidazo[1,2-a]pyridine core pi-systems.

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