4.8 Article

Ligand-Enabled Methylene C(sp3)-H Bond Activation with a Pd(II) Catalyst

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 45, Pages 18570-18572

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja309325e

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Funding

  1. Scripps Research Institute
  2. National Institutes of Health (NIGMS) [1 R01 GM084019-02]
  3. Eli Lilly
  4. Bristol-Myers Squibb
  5. Agency for Science, Technology and Research (A*STAR) Singapore
  6. Astellas Pharma Inc.

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Pd(II) insertion into beta-methylene C(sp(3))-H bonds was enabled by a mutually repulsive and electron-rich quinoline ligand. Ligand tuning led to the development or a method that allows for installation of an aryl,, group On a range of acyclic and cyclic amides containing beta-methylene C(sp(3))-H bonds.

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