4.8 Article

O-Acetyl Oximes as Transformable Directing Groups for Pd-Catalyzed C-H Bond Functionalization

Journal

ORGANIC LETTERS
Volume 12, Issue 3, Pages 532-535

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol902720d

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Funding

  1. NIH NIGMS [GM-073836]
  2. Dupont
  3. AstraZeneca
  4. Merck
  5. Amgen
  6. Abbott
  7. GlaxoSmithKline
  8. Roche
  9. Eli Lilly
  10. Bristol Myers Squibb

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O-Acetyl oximes serve as effective directing groups for Pd-catalyzed sp(2) and sp(3) C-H functionalization reactions. The C-H functionalization products can be subsequently transformed into ortho- or beta-functionalized ketones, alcohols, amines, and heterocycles.

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