4.7 Article

Regioselective Halogenations and Subsequent Suzuki-Miyaura Coupling onto Bicyclic 2-Pyridones

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 3, Pages 972-975

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo902458g

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Funding

  1. Swedish Research Council, Knut
  2. Alice Wallenberg Foundation
  3. JC Kempe Foundation

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A selective synthesis of 6-brorno-8-iodo dihydro thiazolo ring-fused 2-pyridones is described. These halogenated 2-pyridones are selectively arylated by sequential Suzuki-Miyaura couplings. This approach call advantageously be used to synthesize focused libraries of substituted ring-fused 2-pyridones, a class of compounds with novel antibacterial properties.

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