4.8 Article

New Ligands That Promote Cross-Coupling Reactions between Aryl Halides and Unactivated Arenes

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ORGANIC LETTERS
卷 13, 期 14, 页码 3556-3559

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AMER CHEMICAL SOC
DOI: 10.1021/ol2009208

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资金

  1. National Natural Science Foundation [20802078, 20972160, 20772035]
  2. National Basic Research Program of China [2009CB940900]
  3. Shanghai University [DF2009-02]
  4. Pujiang Talent Plan Project [09PJ1409200]
  5. National Major Scientific and Technological Program for Drug Discovery [2009ZX-09103-101]

向作者/读者索取更多资源

Several ligands were designed to promote transition-metal-free cross-coupling reactions of aryl halides with benzene derivatives. Among the systems probed, quinoline-1-amino-2-carboxylic acid was found to serve as an excellent catalyst for cross-coupling between aryl halides and unactivated benzene. Reactions using this inexpensive catalytic system displayed a high functional group tolerance as well as excellent chemoselectivities.

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